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rs121909048

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909048(C;C)
Make rs121909048(C;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position67165827
GeneHSF4
is asnp
is mentioned by
dbSNPrs121909048
ebirs121909048
HLIrs121909048
Exacrs121909048
Varsomers121909048
Maprs121909048
PheGenIrs121909048
hapmaprs121909048
1000 genomesrs121909048
hgdprs121909048
ensemblrs121909048
gopubmedrs121909048
geneviewrs121909048
scholarrs121909048
googlers121909048
pharmgkbrs121909048
gwascentralrs121909048
openSNPrs121909048
23andMers121909048
23andMe allrs121909048
SNP Nexus

SNPshotrs121909048
SNPdbers121909048
MSV3drs121909048
GWAS Ctlgrs121909048
Max Magnitude0
OMIM602438
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909048(C;C)
Alt rs121909048(C;C)
Reference rs121909048(T;T)
Significance Pathogenic
Disease Cataract
Variation info
Gene HSF4
CLNDBN Cataract, zonular
Reversed 0
HGVS NC_000016.9:g.67199730T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000007509.3,