rs111784356

Orientation

plus

Stabilized

plus

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

Make rs111784356(A;A)

Make rs111784356(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

101229574

Gene

IMPG2

is a	snp
is	mentioned by
dbSNP	rs111784356
dbSNP (classic)	rs111784356
ClinGen	rs111784356
ebi	rs111784356
HLI	rs111784356
Exac	rs111784356
Gnomad	rs111784356
Varsome	rs111784356
LitVar	rs111784356
Map	rs111784356
PheGenI	rs111784356
Biobank	rs111784356
1000 genomes	rs111784356
hgdp	rs111784356
ensembl	rs111784356
geneview	rs111784356
scholar	rs111784356
google	rs111784356
pharmgkb	rs111784356
gwascentral	rs111784356
openSNP	rs111784356
23andMe	rs111784356
SNPshot	rs111784356
SNPdbe	rs111784356
MSV3d	rs111784356
GWAS Ctlg	rs111784356

Max Magnitude

0

ClinVar
Risk	rs111784356(A;A)
Alt	rs111784356(A;A)
Reference	Rs111784356(G;G)
Significance	Probable-non-pathogenic
Disease	not specified
Variation	info
Gene	IMPG2
CLNDBN	not specified
Reversed	0
HGVS	NC_000003.11:g.100948418G>A
CLNSRC
CLNACC	RCV000171365.2,