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rs387907337

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907337(C;T)
Make rs387907337(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position111911667
GeneCRYAB, HSPB2, HSPB2-C11orf52
is asnp
is mentioned by
dbSNPrs387907337
ebirs387907337
HLIrs387907337
Exacrs387907337
Varsomers387907337
Maprs387907337
PheGenIrs387907337
hapmaprs387907337
1000 genomesrs387907337
hgdprs387907337
ensemblrs387907337
gopubmedrs387907337
geneviewrs387907337
scholarrs387907337
googlers387907337
pharmgkbrs387907337
gwascentralrs387907337
openSNPrs387907337
23andMers387907337
23andMe allrs387907337
SNP Nexus

SNPshotrs387907337
SNPdbers387907337
MSV3drs387907337
GWAS Ctlgrs387907337
Max Magnitude0
ClinVar
Risk rs387907337(T;T)
Alt rs387907337(T;T)
Reference rs387907337(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.111782391G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000034841.29,