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rs121909050

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121909050(A;G)
Make rs121909050(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position67165742
GeneHSF4
is asnp
is mentioned by
dbSNPrs121909050
ebirs121909050
HLIrs121909050
Exacrs121909050
Varsomers121909050
Maprs121909050
PheGenIrs121909050
hapmaprs121909050
1000 genomesrs121909050
hgdprs121909050
ensemblrs121909050
gopubmedrs121909050
geneviewrs121909050
scholarrs121909050
googlers121909050
pharmgkbrs121909050
gwascentralrs121909050
openSNPrs121909050
23andMers121909050
23andMe allrs121909050
SNP Nexus

SNPshotrs121909050
SNPdbers121909050
MSV3drs121909050
GWAS Ctlgrs121909050
Max Magnitude0
OMIM602438
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121909050(G;G)
Alt rs121909050(G;G)
Reference rs121909050(A;A)
Significance Pathogenic
Disease Cataract
Variation info
Gene HSF4
CLNDBN Cataract, zonular
Reversed 0
HGVS NC_000016.9:g.67199645A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007512.3,