Have questions? Visit https://www.reddit.com/r/SNPedia

rs387906897

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906897(C;C)
Make rs387906897(C;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position44160366
GeneJPH2
is asnp
is mentioned by
dbSNPrs387906897
ebirs387906897
HLIrs387906897
Exacrs387906897
Varsomers387906897
Maprs387906897
PheGenIrs387906897
hapmaprs387906897
1000 genomesrs387906897
hgdprs387906897
ensemblrs387906897
gopubmedrs387906897
geneviewrs387906897
scholarrs387906897
googlers387906897
pharmgkbrs387906897
gwascentralrs387906897
openSNPrs387906897
23andMers387906897
23andMe allrs387906897
SNP Nexus

SNPshotrs387906897
SNPdbers387906897
MSV3drs387906897
GWAS Ctlgrs387906897
Max Magnitude0
ClinVar
Risk rs387906897(C;C)
Alt rs387906897(C;C)
Reference rs387906897(T;T)
Significance Pathogenic
Disease Familial hypertrophic cardiomyopathy 17
Variation info
Gene JPH2
CLNDBN Familial hypertrophic cardiomyopathy 17
Reversed 1
HGVS NC_000020.10:g.42789006A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023409.2,