rs1002820022

Orientation

plus

Stabilized

plus

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

Make rs1002820022(A;A)

Make rs1002820022(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

50054994

Gene

NRXN1

is a	snp
is	mentioned by
dbSNP	rs1002820022
dbSNP (classic)	rs1002820022
ClinGen	rs1002820022
ebi	rs1002820022
HLI	rs1002820022
Exac	rs1002820022
Gnomad	rs1002820022
Varsome	rs1002820022
LitVar	rs1002820022
Map	rs1002820022
PheGenI	rs1002820022
Biobank	rs1002820022
1000 genomes	rs1002820022
hgdp	rs1002820022
ensembl	rs1002820022
geneview	rs1002820022
scholar	rs1002820022
google	rs1002820022
pharmgkb	rs1002820022
gwascentral	rs1002820022
openSNP	rs1002820022
23andMe	rs1002820022
SNPshot	rs1002820022
SNPdbe	rs1002820022
MSV3d	rs1002820022
GWAS Ctlg	rs1002820022

Max Magnitude

0

ClinVar
Risk	rs1002820022(A;A) rs1002820022(T;T)
Alt	rs1002820022(A;A) rs1002820022(T;T)
Reference	Rs1002820022(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	NRXN1
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.50282132G>A
CLNSRC
CLNACC	RCV000480371.1,