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rs121909597

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909597(A;A)
Make rs121909597(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position208124255
GeneCRYGD, ZNF224
is asnp
is mentioned by
dbSNPrs121909597
ebirs121909597
HLIrs121909597
Exacrs121909597
Varsomers121909597
Maprs121909597
PheGenIrs121909597
hapmaprs121909597
1000 genomesrs121909597
hgdprs121909597
ensemblrs121909597
gopubmedrs121909597
geneviewrs121909597
scholarrs121909597
googlers121909597
pharmgkbrs121909597
gwascentralrs121909597
openSNPrs121909597
23andMers121909597
23andMe allrs121909597
SNP Nexus

SNPshotrs121909597
SNPdbers121909597
MSV3drs121909597
GWAS Ctlgrs121909597
Max Magnitude0
OMIM123690
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121909597(A;A)
Alt rs121909597(A;A)
Reference rs121909597(C;C)
Significance Pathogenic
Disease Cataract 4
Variation info
Gene LOC100507443 CRYGD
CLNDBN Cataract 4
Reversed 1
HGVS NC_000002.11:g.208988979G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000018447.26,