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rs864309697

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864309697(A;A)
Make rs864309697(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position25229472
GeneCRYBB2
is asnp
is mentioned by
dbSNPrs864309697
ebirs864309697
HLIrs864309697
Exacrs864309697
Varsomers864309697
Maprs864309697
PheGenIrs864309697
hapmaprs864309697
1000 genomesrs864309697
hgdprs864309697
ensemblrs864309697
gopubmedrs864309697
geneviewrs864309697
scholarrs864309697
googlers864309697
pharmgkbrs864309697
gwascentralrs864309697
openSNPrs864309697
23andMers864309697
23andMe allrs864309697
SNP Nexus

SNPshotrs864309697
SNPdbers864309697
MSV3drs864309697
GWAS Ctlgrs864309697
Max Magnitude0
ClinVar
Risk rs864309697(A;A)
Alt rs864309697(A;A)
Reference rs864309697(C;C)
Significance Probable-Pathogenic
Disease Congenital cataract
Variation info
Gene CRYBB2
CLNDBN Congenital cataract
Reversed 0
HGVS NC_000022.10:g.25625439C>A
CLNSRC
CLNACC RCV000203383.1,