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rs1064793935

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome22
Position26616149
GeneCRYBA4, CRYBB1
is asnp
is mentioned by
dbSNPrs1064793935
dbSNP (old)rs1064793935
ClinGenrs1064793935
ebirs1064793935
HLIrs1064793935
Exacrs1064793935
Gnomadrs1064793935
Varsomers1064793935
Maprs1064793935
PheGenIrs1064793935
Biobankrs1064793935
1000 genomesrs1064793935
hgdprs1064793935
ensemblrs1064793935
gopubmedrs1064793935
geneviewrs1064793935
scholarrs1064793935
googlers1064793935
pharmgkbrs1064793935
gwascentralrs1064793935
openSNPrs1064793935
23andMers1064793935
23andMe allrs1064793935
SNPshotrs1064793935
SNPdbers1064793935
MSV3drs1064793935
GWAS Ctlgrs1064793935
Max Magnitude0
ClinVar
Risk rs1064793935(-;-)
Alt rs1064793935(-;-)
Reference Rs1064793935(G;G)
Significance Pathogenic
Disease Cataract not provided
Variation info
Gene CRYBB1
CLNDBN Cataract, congenital nuclear, autosomal recessive 3 not provided
Reversed 1
HGVS NC_000022.10:g.27012113delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000009225.5, RCV000486232.1,