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rs515726230

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs515726230(A;G)
Make rs515726230(G;G)
ReferenceGRCh38 38.1/142
Chromosome14
Position23397187
GeneMYH6
is asnp
is mentioned by
dbSNPrs515726230
ebirs515726230
HLIrs515726230
Exacrs515726230
Varsomers515726230
Maprs515726230
PheGenIrs515726230
hapmaprs515726230
1000 genomesrs515726230
hgdprs515726230
ensemblrs515726230
gopubmedrs515726230
geneviewrs515726230
scholarrs515726230
googlers515726230
pharmgkbrs515726230
gwascentralrs515726230
openSNPrs515726230
23andMers515726230
23andMe allrs515726230
SNP Nexus

SNPshotrs515726230
SNPdbers515726230
MSV3drs515726230
GWAS Ctlgrs515726230
Max Magnitude0
ClinVar
Risk rs515726230(G;G)
Alt rs515726230(G;G)
Reference rs515726230(A;A)
Significance Probable-Pathogenic
Disease Heart
Variation info
Gene MYH6
CLNDBN Heart, malformation of
Reversed 1
HGVS NC_000014.8:g.23866396T>C
CLNSRC ClinVar
CLNACC RCV000128628.1,