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rs267606875

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606875(C;T)
Make rs267606875(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position101242820
GeneIMPG2
is asnp
is mentioned by
dbSNPrs267606875
ebirs267606875
HLIrs267606875
Exacrs267606875
Varsomers267606875
Maprs267606875
PheGenIrs267606875
hapmaprs267606875
1000 genomesrs267606875
hgdprs267606875
ensemblrs267606875
gopubmedrs267606875
geneviewrs267606875
scholarrs267606875
googlers267606875
pharmgkbrs267606875
gwascentralrs267606875
openSNPrs267606875
23andMers267606875
23andMe allrs267606875
SNP Nexus

SNPshotrs267606875
SNPdbers267606875
MSV3drs267606875
GWAS Ctlgrs267606875
Max Magnitude0
ClinVar
Risk rs267606875(T;T)
Alt rs267606875(T;T)
Reference rs267606875(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 56
Variation info
Gene IMPG2
CLNDBN Retinitis pigmentosa 56
Reversed 1
HGVS NC_000003.11:g.100961664G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003727.2,