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rs121908108

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908108(A;A)
Make rs121908108(A;C)
ReferenceGRCh38 38.1/141
Chromosome20
Position31820357
GeneMYLK2
is asnp
is mentioned by
dbSNPrs121908108
ebirs121908108
HLIrs121908108
Exacrs121908108
Varsomers121908108
Maprs121908108
PheGenIrs121908108
hapmaprs121908108
1000 genomesrs121908108
hgdprs121908108
ensemblrs121908108
gopubmedrs121908108
geneviewrs121908108
scholarrs121908108
googlers121908108
pharmgkbrs121908108
gwascentralrs121908108
openSNPrs121908108
23andMers121908108
23andMe allrs121908108
SNP Nexus

SNPshotrs121908108
SNPdbers121908108
MSV3drs121908108
GWAS Ctlgrs121908108
GMAF0.002755
Max Magnitude0
OMIM606566
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121908108(A;A)
Alt rs121908108(A;A)
Reference rs121908108(C;C)
Significance Pathogenic
Disease Cardiomyopathy not specified
Variation info
Gene MYLK2
CLNDBN Cardiomyopathy, hypertrophic, midventricular, digenic not specified
Reversed 0
HGVS NC_000020.10:g.30408160C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000004466.2, RCV000154782.3,