rs796052787

Orientation

minus

Stabilized

minus

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

Make rs796052787(-;-)

Make rs796052787(-;A)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

50496087

Gene

NRXN1

is a	snp
is	mentioned by
dbSNP	rs796052787
dbSNP (classic)	rs796052787
ClinGen	rs796052787
ebi	rs796052787
HLI	rs796052787
Exac	rs796052787
Gnomad	rs796052787
Varsome	rs796052787
LitVar	rs796052787
Map	rs796052787
PheGenI	rs796052787
Biobank	rs796052787
1000 genomes	rs796052787
hgdp	rs796052787
ensembl	rs796052787
geneview	rs796052787
scholar	rs796052787
google	rs796052787
pharmgkb	rs796052787
gwascentral	rs796052787
openSNP	rs796052787
23andMe	rs796052787
SNPshot	rs796052787
SNPdbe	rs796052787
MSV3d	rs796052787
GWAS Ctlg	rs796052787

Max Magnitude

0

ClinVar
Risk	rs796052787(-;-)
Alt	rs796052787(-;-)
Reference	Rs796052787(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	NRXN1
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.50723225delT
CLNSRC
CLNACC	RCV000188305.1,