rs199867882

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs199867882(A;A)

Make rs199867882(A;G)

Reference

GRCh38 38.1/142

Chromosome

3

Position

101231117

Gene

IMPG2

is a	snp
is	mentioned by
dbSNP	rs199867882
dbSNP (classic)	rs199867882
ClinGen	rs199867882
ebi	rs199867882
HLI	rs199867882
Exac	rs199867882
Gnomad	rs199867882
Varsome	rs199867882
LitVar	rs199867882
Map	rs199867882
PheGenI	rs199867882
Biobank	rs199867882
1000 genomes	rs199867882
hgdp	rs199867882
ensembl	rs199867882
geneview	rs199867882
scholar	rs199867882
google	rs199867882
pharmgkb	rs199867882
gwascentral	rs199867882
openSNP	rs199867882
23andMe	rs199867882
SNPshot	rs199867882
SNPdbe	rs199867882
MSV3d	rs199867882
GWAS Ctlg	rs199867882

Max Magnitude

0

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,