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rs121909596

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909596(A;A)
Make rs121909596(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position208124188
GeneCRYGD, ZNF224
is asnp
is mentioned by
dbSNPrs121909596
ebirs121909596
HLIrs121909596
Exacrs121909596
Varsomers121909596
Maprs121909596
PheGenIrs121909596
hapmaprs121909596
1000 genomesrs121909596
hgdprs121909596
ensemblrs121909596
gopubmedrs121909596
geneviewrs121909596
scholarrs121909596
googlers121909596
pharmgkbrs121909596
gwascentralrs121909596
openSNPrs121909596
23andMers121909596
23andMe allrs121909596
SNP Nexus

SNPshotrs121909596
SNPdbers121909596
MSV3drs121909596
GWAS Ctlgrs121909596
Max Magnitude0
OMIM123690
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121909596(A;A)
Alt rs121909596(A;A)
Reference rs121909596(G;G)
Significance Pathogenic
Disease Cataract 4
Variation info
Gene LOC100507443 CRYGD
CLNDBN Cataract 4
Reversed 1
HGVS NC_000002.11:g.208988912C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000018446.31,