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rs3218716

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3218716(A;A)
Make rs3218716(A;G)
ReferenceGRCh38 38.1/142
Chromosome14
Position23425316
GeneMYH7
is asnp
is mentioned by
dbSNPrs3218716
ebirs3218716
HLIrs3218716
Exacrs3218716
Varsomers3218716
Maprs3218716
PheGenIrs3218716
hapmaprs3218716
1000 genomesrs3218716
hgdprs3218716
ensemblrs3218716
gopubmedrs3218716
geneviewrs3218716
scholarrs3218716
googlers3218716
pharmgkbrs3218716
gwascentralrs3218716
openSNPrs3218716
23andMers3218716
23andMe allrs3218716
SNP Nexus

SNPshotrs3218716
SNPdbers3218716
MSV3drs3218716
GWAS Ctlgrs3218716
Max Magnitude0
? (A;A) (A;G) (G;G) 28


ClinVar
Risk rs3218716(A;A)
Alt rs3218716(A;A)
Reference rs3218716(G;G)
Significance Other
Disease Primary familial hypertrophic cardiomyopathy not provided Familial hypertrophic cardiomyopathy 1
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy not provided Familial hypertrophic cardiomyopathy 1
Reversed 1
HGVS NC_000014.8:g.23894525C>T
CLNSRC ClinVar University of Washington
CLNACC RCV000035790.6, RCV000158532.2, RCV000168872.2,