rs1057520406

Orientation

minus

Stabilized

minus

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

Make rs1057520406(A;G)

Make rs1057520406(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

50091496

Gene

NRXN1

is a	snp
is	mentioned by
dbSNP	rs1057520406
dbSNP (classic)	rs1057520406
ClinGen	rs1057520406
ebi	rs1057520406
HLI	rs1057520406
Exac	rs1057520406
Gnomad	rs1057520406
Varsome	rs1057520406
LitVar	rs1057520406
Map	rs1057520406
PheGenI	rs1057520406
Biobank	rs1057520406
1000 genomes	rs1057520406
hgdp	rs1057520406
ensembl	rs1057520406
geneview	rs1057520406
scholar	rs1057520406
google	rs1057520406
pharmgkb	rs1057520406
gwascentral	rs1057520406
openSNP	rs1057520406
23andMe	rs1057520406
SNPshot	rs1057520406
SNPdbe	rs1057520406
MSV3d	rs1057520406
GWAS Ctlg	rs1057520406

Max Magnitude

0

ClinVar
Risk	rs1057520406(G;G)
Alt	rs1057520406(G;G)
Reference	Rs1057520406(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	NRXN1
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.50318634T>C
CLNSRC
CLNACC	RCV000441331.1,