rs878853357

Orientation

minus

Stabilized

minus

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

Make rs878853357(G;T)

Make rs878853357(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

101228876

Gene

IMPG2

is a	snp
is	mentioned by
dbSNP	rs878853357
dbSNP (classic)	rs878853357
ClinGen	rs878853357
ebi	rs878853357
HLI	rs878853357
Exac	rs878853357
Gnomad	rs878853357
Varsome	rs878853357
LitVar	rs878853357
Map	rs878853357
PheGenI	rs878853357
Biobank	rs878853357
1000 genomes	rs878853357
hgdp	rs878853357
ensembl	rs878853357
geneview	rs878853357
scholar	rs878853357
google	rs878853357
pharmgkb	rs878853357
gwascentral	rs878853357
openSNP	rs878853357
23andMe	rs878853357
SNPshot	rs878853357
SNPdbe	rs878853357
MSV3d	rs878853357
GWAS Ctlg	rs878853357

Max Magnitude

0

ClinVar
Risk	rs878853357(T;T)
Alt	rs878853357(T;T)
Reference	Rs878853357(G;G)
Significance	Probable-Pathogenic
Disease	Retinal dystrophy
Variation	info
Gene	IMPG2
CLNDBN	Retinal dystrophy
Reversed	1
HGVS	NC_000003.11:g.100947720C>A
CLNSRC
CLNACC	RCV000225458.1,