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rs28937573

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs28937573(C;T)
Make rs28937573(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position67165841
GeneHSF4
is asnp
is mentioned by
dbSNPrs28937573
ebirs28937573
HLIrs28937573
Exacrs28937573
Varsomers28937573
Maprs28937573
PheGenIrs28937573
hapmaprs28937573
1000 genomesrs28937573
hgdprs28937573
ensemblrs28937573
gopubmedrs28937573
geneviewrs28937573
scholarrs28937573
googlers28937573
pharmgkbrs28937573
gwascentralrs28937573
openSNPrs28937573
23andMers28937573
23andMe allrs28937573
SNP Nexus

SNPshotrs28937573
SNPdbers28937573
MSV3drs28937573
GWAS Ctlgrs28937573
Max Magnitude0
OMIM602438
DescCATARACT, MARNER TYPE
Variant0002
Relatedalso
Neighborrs28937572
Distance17


ClinVar
Risk rs28937573(T;T)
Alt rs28937573(T;T)
Reference rs28937573(C;C)
Significance Pathogenic
Disease Cataract
Variation info
Gene HSF4
CLNDBN Cataract, zonular
Reversed 0
HGVS NC_000016.9:g.67199744C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007510.3,