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rs376897125

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs376897125(C;T)
Make rs376897125(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23430601
GeneMYH7
is asnp
is mentioned by
dbSNPrs376897125
ebirs376897125
HLIrs376897125
Exacrs376897125
Varsomers376897125
Maprs376897125
PheGenIrs376897125
hapmaprs376897125
1000 genomesrs376897125
hgdprs376897125
ensemblrs376897125
gopubmedrs376897125
geneviewrs376897125
scholarrs376897125
googlers376897125
pharmgkbrs376897125
gwascentralrs376897125
openSNPrs376897125
23andMers376897125
23andMe allrs376897125
SNP Nexus

SNPshotrs376897125
SNPdbers376897125
MSV3drs376897125
GWAS Ctlgrs376897125
Max Magnitude0
ClinVar
Risk rs376897125(T;T)
Alt rs376897125(T;T)
Reference rs376897125(C;C)
Significance Other
Disease Primary familial hypertrophic cardiomyopathy not specified Familial hypertrophic cardiomyopathy 1 not provided
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy not specified Familial hypertrophic cardiomyopathy 1 not provided
Reversed 0
HGVS NC_000014.8:g.23899810C>T
CLNSRC
CLNACC RCV000148711.3, RCV000158772.2, RCV000201440.1, RCV000223879.1,