rs1064795493

Orientation

minus

Stabilized

minus

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

Chromosome

2

Position

51028155

Gene

NRXN1

is a	snp
is	mentioned by
dbSNP	rs1064795493
dbSNP (classic)	rs1064795493
ClinGen	rs1064795493
ebi	rs1064795493
HLI	rs1064795493
Exac	rs1064795493
Gnomad	rs1064795493
Varsome	rs1064795493
LitVar	rs1064795493
Map	rs1064795493
PheGenI	rs1064795493
Biobank	rs1064795493
1000 genomes	rs1064795493
hgdp	rs1064795493
ensembl	rs1064795493
geneview	rs1064795493
scholar	rs1064795493
google	rs1064795493
pharmgkb	rs1064795493
gwascentral	rs1064795493
openSNP	rs1064795493
23andMe	rs1064795493
SNPshot	rs1064795493
SNPdbe	rs1064795493
MSV3d	rs1064795493
GWAS Ctlg	rs1064795493

Max Magnitude

0

ClinVar
Risk	rs1064795493(A;A)
Alt	rs1064795493(A;A)
Reference	Rs1064795493(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	NRXN1
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.51255293C>T
CLNSRC
CLNACC	RCV000484849.1,