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rs786204851

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204851(C;C)
Make rs786204851(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position60509508
GeneSIX6
is asnp
is mentioned by
dbSNPrs786204851
ebirs786204851
HLIrs786204851
Exacrs786204851
Varsomers786204851
Maprs786204851
PheGenIrs786204851
hapmaprs786204851
1000 genomesrs786204851
hgdprs786204851
ensemblrs786204851
gopubmedrs786204851
geneviewrs786204851
scholarrs786204851
googlers786204851
pharmgkbrs786204851
gwascentralrs786204851
openSNPrs786204851
23andMers786204851
23andMe allrs786204851
SNP Nexus

SNPshotrs786204851
SNPdbers786204851
MSV3drs786204851
GWAS Ctlgrs786204851
Max Magnitude0
ClinVar
Risk rs786204851(C;C)
Alt rs786204851(C;C)
Reference rs786204851(T;T)
Significance Pathogenic
Disease Cataract
Variation info
Gene SIX6
CLNDBN Cataract, microphthalmia and nystagmus
Reversed 0
HGVS NC_000014.8:g.60976226T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000169774.3,