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rs387907338

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907338(C;T)
Make rs387907338(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position111911559
GeneCRYAB, HSPB2, HSPB2-C11orf52
is asnp
is mentioned by
dbSNPrs387907338
ebirs387907338
HLIrs387907338
Exacrs387907338
Varsomers387907338
Maprs387907338
PheGenIrs387907338
hapmaprs387907338
1000 genomesrs387907338
hgdprs387907338
ensemblrs387907338
gopubmedrs387907338
geneviewrs387907338
scholarrs387907338
googlers387907338
pharmgkbrs387907338
gwascentralrs387907338
openSNPrs387907338
23andMers387907338
23andMe allrs387907338
SNP Nexus

SNPshotrs387907338
SNPdbers387907338
MSV3drs387907338
GWAS Ctlgrs387907338
Max Magnitude0
ClinVar
Risk rs387907338(T;T)
Alt rs387907338(T;T)
Reference rs387907338(C;C)
Significance Pathogenic
Disease Cataract 16
Variation info
Gene HSPB2-C11orf52 HSPB2 CRYAB
CLNDBN Cataract 16, multiple types
Reversed 1
HGVS NC_000011.9:g.111782283G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000034842.25,