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rs147344332

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs147344332(G;G)
Make rs147344332(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position25231737
GeneCRYBB2
is asnp
is mentioned by
dbSNPrs147344332
ebirs147344332
HLIrs147344332
Exacrs147344332
Varsomers147344332
Maprs147344332
PheGenIrs147344332
hapmaprs147344332
1000 genomesrs147344332
hgdprs147344332
ensemblrs147344332
gopubmedrs147344332
geneviewrs147344332
scholarrs147344332
googlers147344332
pharmgkbrs147344332
gwascentralrs147344332
openSNPrs147344332
23andMers147344332
23andMe allrs147344332
SNP Nexus

SNPshotrs147344332
SNPdbers147344332
MSV3drs147344332
GWAS Ctlgrs147344332
Max Magnitude0
ClinVar
Risk rs147344332(G;G)
Alt rs147344332(G;G)
Reference rs147344332(T;T)
Significance Probable-Pathogenic
Disease Congenital cataract
Variation info
Gene CRYBB2
CLNDBN Congenital cataract
Reversed 0
HGVS NC_000022.10:g.25627704T>G
CLNSRC
CLNACC RCV000203336.1,