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rs387907336

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907336(A;A)
Make rs387907336(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position111908874
GeneCRYAB
is asnp
is mentioned by
dbSNPrs387907336
ebirs387907336
HLIrs387907336
Exacrs387907336
Varsomers387907336
Maprs387907336
PheGenIrs387907336
hapmaprs387907336
1000 genomesrs387907336
hgdprs387907336
ensemblrs387907336
gopubmedrs387907336
geneviewrs387907336
scholarrs387907336
googlers387907336
pharmgkbrs387907336
gwascentralrs387907336
openSNPrs387907336
23andMers387907336
23andMe allrs387907336
SNP Nexus

SNPshotrs387907336
SNPdbers387907336
MSV3drs387907336
GWAS Ctlgrs387907336
Max Magnitude0
ClinVar
Risk rs387907336(A;A)
Alt rs387907336(A;A)
Reference rs387907336(G;G)
Significance Pathogenic
Disease Cataract 16
Variation info
Gene CRYAB
CLNDBN Cataract 16, multiple types
Reversed 1
HGVS NC_000011.9:g.111779598C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000034840.29,