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rs145677314

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs145677314(A;A)
Make rs145677314(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23425346
GeneMYH7
is asnp
is mentioned by
dbSNPrs145677314
ebirs145677314
HLIrs145677314
Exacrs145677314
Varsomers145677314
Maprs145677314
PheGenIrs145677314
hapmaprs145677314
1000 genomesrs145677314
hgdprs145677314
ensemblrs145677314
gopubmedrs145677314
geneviewrs145677314
scholarrs145677314
googlers145677314
pharmgkbrs145677314
gwascentralrs145677314
openSNPrs145677314
23andMers145677314
23andMe allrs145677314
SNP Nexus

SNPshotrs145677314
SNPdbers145677314
MSV3drs145677314
GWAS Ctlgrs145677314
Max Magnitude0
ClinVar
Risk rs145677314(A;A)
Alt rs145677314(A;A)
Reference rs145677314(G;G)
Significance Other
Disease Primary familial hypertrophic cardiomyopathy not specified Hypertrophic cardiomyopathy
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy not specified Hypertrophic cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23894555G>A
CLNSRC
CLNACC RCV000148709.2, RCV000154774.3, RCV000231165.1,