rs797044930

Orientation

minus

Stabilized

minus

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

Make rs797044930(C;T)

Make rs797044930(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

13608697

Gene	GRIN2B, LOC105369668

is a	snp
is	mentioned by
dbSNP	rs797044930
dbSNP (classic)	rs797044930
ClinGen	rs797044930
ebi	rs797044930
HLI	rs797044930
Exac	rs797044930
Gnomad	rs797044930
Varsome	rs797044930
LitVar	rs797044930
Map	rs797044930
PheGenI	rs797044930
Biobank	rs797044930
1000 genomes	rs797044930
hgdp	rs797044930
ensembl	rs797044930
geneview	rs797044930
scholar	rs797044930
google	rs797044930
pharmgkb	rs797044930
gwascentral	rs797044930
openSNP	rs797044930
23andMe	rs797044930
SNPshot	rs797044930
SNPdbe	rs797044930
MSV3d	rs797044930
GWAS Ctlg	rs797044930

Max Magnitude

0

ClinVar
Risk	rs797044930(T;T)
Alt	rs797044930(T;T)
Reference	Rs797044930(C;C)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	GRIN2B
CLNDBN	Inborn genetic diseases
Reversed	1
HGVS	NC_000012.11:g.13761631G>A
CLNSRC
CLNACC	RCV000190769.1,