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rs730880961

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880961(C;T)
Make rs730880961(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position46860703
GeneMYL3
is asnp
is mentioned by
dbSNPrs730880961
ebirs730880961
HLIrs730880961
Exacrs730880961
Varsomers730880961
Maprs730880961
PheGenIrs730880961
hapmaprs730880961
1000 genomesrs730880961
hgdprs730880961
ensemblrs730880961
gopubmedrs730880961
geneviewrs730880961
scholarrs730880961
googlers730880961
pharmgkbrs730880961
gwascentralrs730880961
openSNPrs730880961
23andMers730880961
23andMe allrs730880961
SNP Nexus

SNPshotrs730880961
SNPdbers730880961
MSV3drs730880961
GWAS Ctlgrs730880961
Max Magnitude0
ClinVar
Risk rs730880961(T;T)
Alt rs730880961(T;T)
Reference rs730880961(C;C)
Significance Pathogenic
Disease not specified Hypertrophic cardiomyopathy
Variation info
Gene MYL3
CLNDBN not specified Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000003.11:g.46902193G>A
CLNSRC
CLNACC RCV000158961.2, RCV000233649.1,