GWAS Catalog

 G MYLK

Description: myosin light chain kinase
Location: 3:123610049-123884332 Cytogenetic region: 3q21.1 Biotype: protein coding

Associations 19   Studies 18

 G MYLK-AS1

Description: MYLK antisense RNA 1
Location: 3:123584354-123716399 Cytogenetic region: 3q21.1 Biotype: lncRNA

Associations 10   Studies 10

 V rs35919256

Location: 3:123837324 Cytogenetic region:3q21.1 Most severe consequence: Intron variant Mapped gene(s): MYLK

Associations 1   Studies 1

 V rs1343700

Location: 3:123852907 Cytogenetic region:3q21.1 Most severe consequence: Intron variant Mapped gene(s): MYLK

Associations 1   Studies 1

 V rs2682204

Location: 3:123837617 Cytogenetic region:3q21.1 Most severe consequence: Intron variant Mapped gene(s): MYLK

Associations 1   Studies 1

 V rs34067381

Location: 3:123875572 Cytogenetic region:3q21.1 Most severe consequence: Intron variant Mapped gene(s): MYLK

Associations 1   Studies 1

 V rs6783507

Location: 3:123799411 Cytogenetic region:3q21.1 Most severe consequence: Intron variant Mapped gene(s): MYLK

Associations 1   Studies 1

 V rs2700352

Location: 3:123831616 Cytogenetic region:3q21.1 Most severe consequence: 5 prime utr variant Mapped gene(s): MYLK

Associations 1   Studies 1

 V rs11409032

Location: 3:123848255 Cytogenetic region:3q21.1 Most severe consequence: Intron variant Mapped gene(s): MYLK

Associations 1   Studies 1

 V rs554511356

Location: 3:123799590 Cytogenetic region:3q21.1 Most severe consequence: Intron variant Mapped gene(s): MYLK

Associations 1   Studies 1

 V rs188930018

Location: 3:123828025 Cytogenetic region:3q21.1 Most severe consequence: Intron variant Mapped gene(s): MYLK

Associations 1   Studies 1

 V rs117628897

Location: 3:123862829 Cytogenetic region:3q21.1 Most severe consequence: Intron variant Mapped gene(s): MYLK

Associations 1   Studies 1

 V rs4297993

Location: 3:123676908 Cytogenetic region:3q21.1 Most severe consequence: Intron variant Mapped gene(s): MYLK-AS1,MYLK

Associations 1   Studies 1

 V rs820371

Location: 3:123685864 Cytogenetic region:3q21.1 Most severe consequence: Intron variant Mapped gene(s): MYLK-AS1,MYLK

Associations 1   Studies 1

 V rs2605419

Location: 3:123695582 Cytogenetic region:3q21.1 Most severe consequence: Intron variant Mapped gene(s): MYLK-AS1,MYLK

Associations 1   Studies 1

 V rs820335

Location: 3:123696667 Cytogenetic region:3q21.1 Most severe consequence: Intron variant Mapped gene(s): MYLK-AS1,MYLK

Associations 1   Studies 1

 V rs865358

Location: 3:123700066 Cytogenetic region:3q21.1 Most severe consequence: Missense variant Mapped gene(s): MYLK-AS1,MYLK

Associations 1   Studies 1

 V rs168845

Location: 3:123705793 Cytogenetic region:3q21.1 Most severe consequence: Intron variant Mapped gene(s): MYLK-AS1,MYLK

Associations 1   Studies 1

 V rs820343

Location: 3:123713665 Cytogenetic region:3q21.1 Most severe consequence: Intron variant Mapped gene(s): MYLK-AS1,MYLK

Associations 1   Studies 1

 V rs820324

Location: 3:123663984 Cytogenetic region:3q21.1 Most severe consequence: Intron variant Mapped gene(s): MYLK-AS1,MYLK

Associations 1   Studies 1

 V rs72626347

Location: 3:123668019 Cytogenetic region:3q21.1 Most severe consequence: Intron variant Mapped gene(s): MYLK-AS1,MYLK

Associations 1   Studies 1

 V rs848145

Location: 3:123618135 Cytogenetic region:3q21.1 Most severe consequence: 3 prime utr variant Mapped gene(s): MYLK-AS1,MYLK

Associations 1   Studies 1

 V rs147182004

Location: 3:123635023 Cytogenetic region:3q21.1 Most severe consequence: Intron variant Mapped gene(s): MYLK-AS1,MYLK

Associations 1   Studies 1

 V rs12637836

Location: 3:123676078 Cytogenetic region:3q21.1 Most severe consequence: Intron variant Mapped gene(s): MYLK-AS1,MYLK

Associations 1   Studies 1

 V rs820360

Location: 3:123674286 Cytogenetic region:3q21.1 Most severe consequence: Intron variant Mapped gene(s): MYLK-AS1,MYLK

Associations 1   Studies 1

 V rs75085211

Location: 3:123585847 Cytogenetic region:3q21.1 Most severe consequence: Regulatory region variant Mapped gene(s): MYLK-AS1

Associations 1   Studies 1

 V rs2091661

Location: 3:123891496 Cytogenetic region:3q21.1 Most severe consequence: Intergenic variant Mapped gene(s): CCDC14,MYLK

Associations 1   Studies 1

 V rs116197893

Location: 3:123590888 Cytogenetic region:3q21.1 Most severe consequence: Intergenic variant Mapped gene(s): MYLK-AS1

Associations 1   Studies 1

 G MYLKP2

Description: MYLK pseudogene 2
Location: 3:125681305-125681453 Cytogenetic region: 3q21.2 Biotype: transcribed processed pseudogene

Associations 4   Studies 3