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rs398122944

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122944(A;A)
Make rs398122944(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position208128257
GeneCRYGC, LOC100507443
is asnp
is mentioned by
dbSNPrs398122944
ebirs398122944
HLIrs398122944
Exacrs398122944
Varsomers398122944
Maprs398122944
PheGenIrs398122944
hapmaprs398122944
1000 genomesrs398122944
hgdprs398122944
ensemblrs398122944
gopubmedrs398122944
geneviewrs398122944
scholarrs398122944
googlers398122944
pharmgkbrs398122944
gwascentralrs398122944
openSNPrs398122944
23andMers398122944
23andMe allrs398122944
SNP Nexus

SNPshotrs398122944
SNPdbers398122944
MSV3drs398122944
GWAS Ctlgrs398122944
Max Magnitude0
ClinVar
Risk rs398122944(A;A)
Alt rs398122944(A;A)
Reference rs398122944(G;G)
Significance Pathogenic
Disease Cataract
Variation info
Gene CRYGC LOC100507443
CLNDBN Cataract, coppock-like
Reversed 1
HGVS NC_000002.11:g.208992981C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000056310.27,