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rs371898076

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs371898076(C;T)
Make rs371898076(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position23426833
GeneMYH7
is asnp
is mentioned by
dbSNPrs371898076
ebirs371898076
HLIrs371898076
Exacrs371898076
Varsomers371898076
Maprs371898076
PheGenIrs371898076
hapmaprs371898076
1000 genomesrs371898076
hgdprs371898076
ensemblrs371898076
gopubmedrs371898076
geneviewrs371898076
scholarrs371898076
googlers371898076
pharmgkbrs371898076
gwascentralrs371898076
openSNPrs371898076
23andMers371898076
23andMe allrs371898076
SNP Nexus

SNPshotrs371898076
SNPdbers371898076
MSV3drs371898076
GWAS Ctlgrs371898076
Max Magnitude0
ClinVar
Risk rs371898076(T;T)
Alt rs371898076(T;T)
Reference rs371898076(C;C)
Significance Other
Disease Primary familial hypertrophic cardiomyopathy not provided Familial hypertrophic cardiomyopathy 1 Hypertrophic cardiomyopathy
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy not provided Familial hypertrophic cardiomyopathy 1 Hypertrophic cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23896042C>T
CLNSRC Centenary Institute
CLNACC RCV000035758.9, RCV000158822.2, RCV000162333.3, RCV000168409.3,