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rs864309682

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864309682(A;A)
Make rs864309682(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position26607953
GeneCRYBA4, CRYBB1
is asnp
is mentioned by
dbSNPrs864309682
ebirs864309682
HLIrs864309682
Exacrs864309682
Varsomers864309682
Maprs864309682
PheGenIrs864309682
hapmaprs864309682
1000 genomesrs864309682
hgdprs864309682
ensemblrs864309682
gopubmedrs864309682
geneviewrs864309682
scholarrs864309682
googlers864309682
pharmgkbrs864309682
gwascentralrs864309682
openSNPrs864309682
23andMers864309682
23andMe allrs864309682
SNP Nexus

SNPshotrs864309682
SNPdbers864309682
MSV3drs864309682
GWAS Ctlgrs864309682
Max Magnitude0
ClinVar
Risk rs864309682(A;A)
Alt rs864309682(A;A)
Reference rs864309682(G;G)
Significance Probable-Pathogenic
Disease Congenital cataract
Variation info
Gene CRYBB1
CLNDBN Congenital cataract
Reversed 1
HGVS NC_000022.10:g.27003917C>T
CLNSRC
CLNACC RCV000203364.1,