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rs74315486

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs74315486(C;C)
Make rs74315486(C;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position26625603
GeneCRYBA4
is asnp
is mentioned by
dbSNPrs74315486
ebirs74315486
HLIrs74315486
Exacrs74315486
Varsomers74315486
Maprs74315486
PheGenIrs74315486
hapmaprs74315486
1000 genomesrs74315486
hgdprs74315486
ensemblrs74315486
gopubmedrs74315486
geneviewrs74315486
scholarrs74315486
googlers74315486
pharmgkbrs74315486
gwascentralrs74315486
openSNPrs74315486
23andMers74315486
23andMe allrs74315486
SNP Nexus

SNPshotrs74315486
SNPdbers74315486
MSV3drs74315486
GWAS Ctlgrs74315486
Max Magnitude0
OMIM123631
Desc
Variant0001
Relatedalso
ClinVar
Risk rs74315486(C;C)
Alt rs74315486(C;C)
Reference rs74315486(T;T)
Significance Pathogenic
Disease Cataract 23
Variation info
Gene CRYBA4
CLNDBN Cataract 23
Reversed 0
HGVS NC_000022.10:g.27021567T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000018455.28,