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rs763538103

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs763538103(A;A)
Make rs763538103(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position23415794
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs763538103
ebirs763538103
HLIrs763538103
Exacrs763538103
Varsomers763538103
Maprs763538103
PheGenIrs763538103
hapmaprs763538103
1000 genomesrs763538103
hgdprs763538103
ensemblrs763538103
gopubmedrs763538103
geneviewrs763538103
scholarrs763538103
googlers763538103
pharmgkbrs763538103
gwascentralrs763538103
openSNPrs763538103
23andMers763538103
23andMe allrs763538103
SNP Nexus

SNPshotrs763538103
SNPdbers763538103
MSV3drs763538103
GWAS Ctlgrs763538103
Max Magnitude0
ClinVar
Risk rs763538103(A,T;A,T)
Alt rs763538103(A,T;A,T)
Reference rs763538103(G;G)
Significance Probable-Pathogenic
Disease Familial hypertrophic cardiomyopathy 1
Variation info
Gene MYH7 MHRT
CLNDBN Familial hypertrophic cardiomyopathy 1
Reversed 0
HGVS NC_000014.8:g.23885003G>T
CLNSRC
CLNACC RCV000201468.1,