rs786205564

Orientation

minus

Stabilized

minus

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

Make rs786205564(A;A)

Make rs786205564(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

101244057

Gene

IMPG2

is a	snp
is	mentioned by
dbSNP	rs786205564
dbSNP (classic)	rs786205564
ClinGen	rs786205564
ebi	rs786205564
HLI	rs786205564
Exac	rs786205564
Gnomad	rs786205564
Varsome	rs786205564
LitVar	rs786205564
Map	rs786205564
PheGenI	rs786205564
Biobank	rs786205564
1000 genomes	rs786205564
hgdp	rs786205564
ensembl	rs786205564
geneview	rs786205564
scholar	rs786205564
google	rs786205564
pharmgkb	rs786205564
gwascentral	rs786205564
openSNP	rs786205564
23andMe	rs786205564
SNPshot	rs786205564
SNPdbe	rs786205564
MSV3d	rs786205564
GWAS Ctlg	rs786205564

Max Magnitude

0

ClinVar
Risk	rs786205564(A;A)
Alt	rs786205564(A;A)
Reference	Rs786205564(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	IMPG2
CLNDBN	not provided
Reversed	1
HGVS	NC_000003.11:g.100962901C>T
CLNSRC
CLNACC	RCV000171366.1,