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rs397515626

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515626(A;A)
Make rs397515626(A;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position43169161
GeneCRYAA
is asnp
is mentioned by
dbSNPrs397515626
ebirs397515626
HLIrs397515626
Exacrs397515626
Varsomers397515626
Maprs397515626
PheGenIrs397515626
hapmaprs397515626
1000 genomesrs397515626
hgdprs397515626
ensemblrs397515626
gopubmedrs397515626
geneviewrs397515626
scholarrs397515626
googlers397515626
pharmgkbrs397515626
gwascentralrs397515626
openSNPrs397515626
23andMers397515626
23andMe allrs397515626
SNP Nexus

SNPshotrs397515626
SNPdbers397515626
MSV3drs397515626
GWAS Ctlgrs397515626
Max Magnitude0
ClinVar
Risk rs397515626(A;A)
Alt rs397515626(A;A)
Reference rs397515626(G;G)
Significance Pathogenic
Disease Cataract
Variation info
Gene LOC102724652 CRYAA
CLNDBN Cataract, autosomal dominant
Reversed 0
HGVS NC_000021.8:g.44589271G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000059330.23,