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rs267606874

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606874(C;G)
Make rs267606874(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position101275694
GeneIMPG2
is asnp
is mentioned by
dbSNPrs267606874
ebirs267606874
HLIrs267606874
Exacrs267606874
Varsomers267606874
Maprs267606874
PheGenIrs267606874
hapmaprs267606874
1000 genomesrs267606874
hgdprs267606874
ensemblrs267606874
gopubmedrs267606874
geneviewrs267606874
scholarrs267606874
googlers267606874
pharmgkbrs267606874
gwascentralrs267606874
openSNPrs267606874
23andMers267606874
23andMe allrs267606874
SNP Nexus

SNPshotrs267606874
SNPdbers267606874
MSV3drs267606874
GWAS Ctlgrs267606874
Max Magnitude0
ClinVar
Risk rs267606874(G;G)
Alt rs267606874(G;G)
Reference rs267606874(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 56
Variation info
Gene IMPG2
CLNDBN Retinitis pigmentosa 56
Reversed 1
HGVS NC_000003.11:g.100994538G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000003724.2,