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rs121909598

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909598(A;A)
Make rs121909598(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position208121728
GeneCRYGD, ZNF224
is asnp
is mentioned by
dbSNPrs121909598
ebirs121909598
HLIrs121909598
Exacrs121909598
Varsomers121909598
Maprs121909598
PheGenIrs121909598
hapmaprs121909598
1000 genomesrs121909598
hgdprs121909598
ensemblrs121909598
gopubmedrs121909598
geneviewrs121909598
scholarrs121909598
googlers121909598
pharmgkbrs121909598
gwascentralrs121909598
openSNPrs121909598
23andMers121909598
23andMe allrs121909598
SNP Nexus

SNPshotrs121909598
SNPdbers121909598
MSV3drs121909598
GWAS Ctlgrs121909598
Max Magnitude0
OMIM123690
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121909598(A;A)
Alt rs121909598(A;A)
Reference rs121909598(G;G)
Significance Pathogenic
Disease Cataract 4
Variation info
Gene LOC100507443 CRYGD
CLNDBN Cataract 4
Reversed 1
HGVS NC_000002.11:g.208986452C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000018450.30,