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rs730880161

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880161(A;A)
Make rs730880161(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424044
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880161
ebirs730880161
HLIrs730880161
Exacrs730880161
Varsomers730880161
Maprs730880161
PheGenIrs730880161
hapmaprs730880161
1000 genomesrs730880161
hgdprs730880161
ensemblrs730880161
gopubmedrs730880161
geneviewrs730880161
scholarrs730880161
googlers730880161
pharmgkbrs730880161
gwascentralrs730880161
openSNPrs730880161
23andMers730880161
23andMe allrs730880161
SNP Nexus

SNPshotrs730880161
SNPdbers730880161
MSV3drs730880161
GWAS Ctlgrs730880161
Max Magnitude0
ClinVar
Risk rs730880161(A;A)
Alt rs730880161(A;A)
Reference rs730880161(G;G)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not provided
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy not provided
Reversed 1
HGVS NC_000014.8:g.23893253C>T
CLNSRC
CLNACC RCV000157362.2, RCV000225718.1,