rs1057521798

Orientation

minus

Stabilized

minus

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

Make rs1057521798(G;G)

Make rs1057521798(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

50497380

Gene

NRXN1

is a	snp
is	mentioned by
dbSNP	rs1057521798
dbSNP (classic)	rs1057521798
ClinGen	rs1057521798
ebi	rs1057521798
HLI	rs1057521798
Exac	rs1057521798
Gnomad	rs1057521798
Varsome	rs1057521798
LitVar	rs1057521798
Map	rs1057521798
PheGenI	rs1057521798
Biobank	rs1057521798
1000 genomes	rs1057521798
hgdp	rs1057521798
ensembl	rs1057521798
geneview	rs1057521798
scholar	rs1057521798
google	rs1057521798
pharmgkb	rs1057521798
gwascentral	rs1057521798
openSNP	rs1057521798
23andMe	rs1057521798
SNPshot	rs1057521798
SNPdbe	rs1057521798
MSV3d	rs1057521798
GWAS Ctlg	rs1057521798

Max Magnitude

0

ClinVar
Risk	rs1057521798(G;G)
Alt	rs1057521798(G;G)
Reference	Rs1057521798(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	NRXN1
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.50724518A>C
CLNSRC
CLNACC	RCV000427988.1,