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rs199867882

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199867882(A;A)
Make rs199867882(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position101231117
GeneIMPG2
is asnp
is mentioned by
dbSNPrs199867882
ebirs199867882
HLIrs199867882
Exacrs199867882
Varsomers199867882
Maprs199867882
PheGenIrs199867882
hapmaprs199867882
1000 genomesrs199867882
hgdprs199867882
ensemblrs199867882
gopubmedrs199867882
geneviewrs199867882
scholarrs199867882
googlers199867882
pharmgkbrs199867882
gwascentralrs199867882
openSNPrs199867882
23andMers199867882
23andMe allrs199867882
SNP Nexus

SNPshotrs199867882
SNPdbers199867882
MSV3drs199867882
GWAS Ctlgrs199867882
Max Magnitude0
ClinVar
Risk rs199867882(A;A)
Alt rs199867882(A;A)
Reference rs199867882(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene IMPG2
CLNDBN Retinitis pigmentosa
Reversed 0
HGVS NC_000003.11:g.100949961G>A
CLNSRC ClinVar
CLNACC RCV000132676.1,