rs876661102

Orientation

minus

Stabilized

minus

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

Make rs876661102(-;-)

Make rs876661102(-;AAG)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

13564310

Gene

GRIN2B

is a	snp
is	mentioned by
dbSNP	rs876661102
dbSNP (classic)	rs876661102
ClinGen	rs876661102
ebi	rs876661102
HLI	rs876661102
Exac	rs876661102
Gnomad	rs876661102
Varsome	rs876661102
LitVar	rs876661102
Map	rs876661102
PheGenI	rs876661102
Biobank	rs876661102
1000 genomes	rs876661102
hgdp	rs876661102
ensembl	rs876661102
geneview	rs876661102
scholar	rs876661102
google	rs876661102
pharmgkb	rs876661102
gwascentral	rs876661102
openSNP	rs876661102
23andMe	rs876661102
SNPshot	rs876661102
SNPdbe	rs876661102
MSV3d	rs876661102
GWAS Ctlg	rs876661102

Max Magnitude

0

ClinVar
Risk	rs876661102(-;-)
Alt	rs876661102(-;-)
Reference	Rs876661102(AAG;AAG)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2B
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.13717244_13717246delCTT
CLNSRC
CLNACC	RCV000223164.1,