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rs781192528

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs781192528(C;T)
Make rs781192528(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position46705321
GeneZNF408
is asnp
is mentioned by
dbSNPrs781192528
ebirs781192528
HLIrs781192528
Exacrs781192528
Varsomers781192528
Maprs781192528
PheGenIrs781192528
hapmaprs781192528
1000 genomesrs781192528
hgdprs781192528
ensemblrs781192528
gopubmedrs781192528
geneviewrs781192528
scholarrs781192528
googlers781192528
pharmgkbrs781192528
gwascentralrs781192528
openSNPrs781192528
23andMers781192528
23andMe allrs781192528
SNP Nexus

SNPshotrs781192528
SNPdbers781192528
MSV3drs781192528
GWAS Ctlgrs781192528
Max Magnitude0
ClinVar
Risk rs781192528(T;T)
Alt rs781192528(T;T)
Reference rs781192528(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 72
Variation info
Gene ZNF408
CLNDBN Retinitis pigmentosa 72
Reversed 0
HGVS NC_000011.9:g.46726871C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000186512.3,