rs797044925

Orientation

plus

Stabilized

plus

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

Make rs797044925(A;A)

Make rs797044925(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

137163668

Gene

GRIN1

is a	snp
is	mentioned by
dbSNP	rs797044925
dbSNP (classic)	rs797044925
ClinGen	rs797044925
ebi	rs797044925
HLI	rs797044925
Exac	rs797044925
Gnomad	rs797044925
Varsome	rs797044925
LitVar	rs797044925
Map	rs797044925
PheGenI	rs797044925
Biobank	rs797044925
1000 genomes	rs797044925
hgdp	rs797044925
ensembl	rs797044925
geneview	rs797044925
scholar	rs797044925
google	rs797044925
pharmgkb	rs797044925
gwascentral	rs797044925
openSNP	rs797044925
23andMe	rs797044925
SNPshot	rs797044925
SNPdbe	rs797044925
MSV3d	rs797044925
GWAS Ctlg	rs797044925

Max Magnitude

0

ClinVar
Risk	rs797044925(A;A)
Alt	rs797044925(A;A)
Reference	Rs797044925(G;G)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	GRIN1
CLNDBN	Inborn genetic diseases
Reversed	0
HGVS	NC_000009.11:g.140058120G>A
CLNSRC
CLNACC	RCV000190763.1,