rs397514555

Orientation

minus

Stabilized

minus

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

Make rs397514555(A;A)

Make rs397514555(A;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

13615626

Gene	GRIN2B, LOC105369668

is a	snp
is	mentioned by
dbSNP	rs397514555
dbSNP (classic)	rs397514555
ClinGen	rs397514555
ebi	rs397514555
HLI	rs397514555
Exac	rs397514555
Gnomad	rs397514555
Varsome	rs397514555
LitVar	rs397514555
Map	rs397514555
PheGenI	rs397514555
Biobank	rs397514555
1000 genomes	rs397514555
hgdp	rs397514555
ensembl	rs397514555
geneview	rs397514555
scholar	rs397514555
google	rs397514555
pharmgkb	rs397514555
gwascentral	rs397514555
openSNP	rs397514555
23andMe	rs397514555
SNPshot	rs397514555
SNPdbe	rs397514555
MSV3d	rs397514555
GWAS Ctlg	rs397514555

Max Magnitude

0

ClinVar
Risk	rs397514555(A;A)
Alt	rs397514555(A;A)
Reference	Rs397514555(G;G)
Significance	Pathogenic
Disease	Mental retardation
Variation	info
Gene	GRIN2B
CLNDBN	Mental retardation, autosomal dominant 6
Reversed	1
HGVS	NC_000012.11:g.13768560C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000032862.28,