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rs267606903

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606903(A;A)
Make rs267606903(A;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position23394294
GeneMYH6
is asnp
is mentioned by
dbSNPrs267606903
ebirs267606903
HLIrs267606903
Exacrs267606903
Varsomers267606903
Maprs267606903
PheGenIrs267606903
hapmaprs267606903
1000 genomesrs267606903
hgdprs267606903
ensemblrs267606903
gopubmedrs267606903
geneviewrs267606903
scholarrs267606903
googlers267606903
pharmgkbrs267606903
gwascentralrs267606903
openSNPrs267606903
23andMers267606903
23andMe allrs267606903
SNP Nexus

SNPshotrs267606903
SNPdbers267606903
MSV3drs267606903
GWAS Ctlgrs267606903
Max Magnitude0
ClinVar
Risk rs267606903(A;A)
Alt rs267606903(A;A)
Reference rs267606903(T;T)
Significance Pathogenic
Disease Atrial septal defect 3
Variation info
Gene MYH6
CLNDBN Atrial septal defect 3
Reversed 1
HGVS NC_000014.8:g.23863503A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015211.25,