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

rs121909049

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909049(A;A)
Make rs121909049(A;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position67164867
GeneHSF4
is asnp
is mentioned by
dbSNPrs121909049
ebirs121909049
HLIrs121909049
Exacrs121909049
Varsomers121909049
Maprs121909049
PheGenIrs121909049
hapmaprs121909049
1000 genomesrs121909049
hgdprs121909049
ensemblrs121909049
gopubmedrs121909049
geneviewrs121909049
scholarrs121909049
googlers121909049
pharmgkbrs121909049
gwascentralrs121909049
openSNPrs121909049
23andMers121909049
23andMe allrs121909049
SNP Nexus

SNPshotrs121909049
SNPdbers121909049
MSV3drs121909049
GWAS Ctlgrs121909049
Max Magnitude0
OMIM602438
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121909049(A;A)
Alt rs121909049(A;A)
Reference rs121909049(C;C)
Significance Pathogenic
Disease Cataract
Variation info
Gene HSF4
CLNDBN Cataract, zonular
Reversed 0
HGVS NC_000016.9:g.67198770C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007511.3,