rs869320773

Orientation

plus

Stabilized

plus

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

Make rs869320773(C;C)

Make rs869320773(C;G)

Reference

GRCh38.p2 38.2/147

Chromosome

4

Position

527231

Gene

PIGG

is a	snp
is	mentioned by
dbSNP	rs869320773
dbSNP (classic)	rs869320773
ClinGen	rs869320773
ebi	rs869320773
HLI	rs869320773
Exac	rs869320773
Gnomad	rs869320773
Varsome	rs869320773
LitVar	rs869320773
Map	rs869320773
PheGenI	rs869320773
Biobank	rs869320773
1000 genomes	rs869320773
hgdp	rs869320773
ensembl	rs869320773
geneview	rs869320773
scholar	rs869320773
google	rs869320773
pharmgkb	rs869320773
gwascentral	rs869320773
openSNP	rs869320773
23andMe	rs869320773
SNPshot	rs869320773
SNPdbe	rs869320773
MSV3d	rs869320773
GWAS Ctlg	rs869320773

Max Magnitude

0

ClinVar
Risk	rs869320773(C;C)
Alt	rs869320773(C;C)
Reference	Rs869320773(G;G)
Significance	Pathogenic
Disease	Mental retardation
Variation	info
Gene	PIGG
CLNDBN	Mental retardation, autosomal recessive 53
Reversed	0
HGVS	NC_000004.11:g.521020G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000210941.1,