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rs370310929

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs370310929(A;A)
Make rs370310929(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23429047
GeneMYH7
is asnp
is mentioned by
dbSNPrs370310929
ebirs370310929
HLIrs370310929
Exacrs370310929
Varsomers370310929
Maprs370310929
PheGenIrs370310929
hapmaprs370310929
1000 genomesrs370310929
hgdprs370310929
ensemblrs370310929
gopubmedrs370310929
geneviewrs370310929
scholarrs370310929
googlers370310929
pharmgkbrs370310929
gwascentralrs370310929
openSNPrs370310929
23andMers370310929
23andMe allrs370310929
SNP Nexus

SNPshotrs370310929
SNPdbers370310929
MSV3drs370310929
GWAS Ctlgrs370310929
Max Magnitude0
ClinVar
Risk rs370310929(A,C;A,C)
Alt rs370310929(A,C;A,C)
Reference rs370310929(T;T)
Significance Pathogenic
Disease not specified Cardiomyopathy
Variation info
Gene MYH7
CLNDBN not specified Cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23898256T>A; NC_000014.8:g.23898256T>C
CLNSRC
CLNACC RCV000154611.2, RCV000158793.1,