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rs864309685

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864309685(G;G)
Make rs864309685(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position43169241
GeneCRYAA
is asnp
is mentioned by
dbSNPrs864309685
ebirs864309685
HLIrs864309685
Exacrs864309685
Varsomers864309685
Maprs864309685
PheGenIrs864309685
hapmaprs864309685
1000 genomesrs864309685
hgdprs864309685
ensemblrs864309685
gopubmedrs864309685
geneviewrs864309685
scholarrs864309685
googlers864309685
pharmgkbrs864309685
gwascentralrs864309685
openSNPrs864309685
23andMers864309685
23andMe allrs864309685
SNP Nexus

SNPshotrs864309685
SNPdbers864309685
MSV3drs864309685
GWAS Ctlgrs864309685
Max Magnitude0
ClinVar
Risk rs864309685(G;G)
Alt rs864309685(G;G)
Reference rs864309685(T;T)
Significance Probable-Pathogenic
Disease Congenital cataract
Variation info
Gene LOC102724652 CRYAA
CLNDBN Congenital cataract
Reversed 0
HGVS NC_000021.8:g.44589351T>G
CLNSRC
CLNACC RCV000203376.1,