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rs104893736

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893736(G;T)
Make rs104893736(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position186539566
GeneCRYGS
is asnp
is mentioned by
dbSNPrs104893736
ebirs104893736
HLIrs104893736
Exacrs104893736
Varsomers104893736
Maprs104893736
PheGenIrs104893736
hapmaprs104893736
1000 genomesrs104893736
hgdprs104893736
ensemblrs104893736
gopubmedrs104893736
geneviewrs104893736
scholarrs104893736
googlers104893736
pharmgkbrs104893736
gwascentralrs104893736
openSNPrs104893736
23andMers104893736
23andMe allrs104893736
SNP Nexus

SNPshotrs104893736
SNPdbers104893736
MSV3drs104893736
GWAS Ctlgrs104893736
Max Magnitude0
OMIM123730
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104893736(T;T)
Alt rs104893736(T;T)
Reference rs104893736(G;G)
Significance Pathogenic
Disease Cataract 20
Variation info
Gene CRYGS
CLNDBN Cataract 20, multiple types
Reversed 1
HGVS NC_000003.11:g.186257355C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018444.28,