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rs767148171

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs767148171(G;G)
Make rs767148171(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position23416941
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs767148171
ebirs767148171
HLIrs767148171
Exacrs767148171
Varsomers767148171
Maprs767148171
PheGenIrs767148171
hapmaprs767148171
1000 genomesrs767148171
hgdprs767148171
ensemblrs767148171
gopubmedrs767148171
geneviewrs767148171
scholarrs767148171
googlers767148171
pharmgkbrs767148171
gwascentralrs767148171
openSNPrs767148171
23andMers767148171
23andMe allrs767148171
SNP Nexus

SNPshotrs767148171
SNPdbers767148171
MSV3drs767148171
GWAS Ctlgrs767148171
Max Magnitude0
ClinVar
Risk rs767148171(G;G)
Alt rs767148171(G;G)
Reference rs767148171(T;T)
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.23886150T>C
CLNSRC
CLNACC RCV000201485.1,