rs1057520844

Orientation

plus

Stabilized

plus

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

Make rs1057520844(A;A)

Make rs1057520844(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

165388710

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs1057520844
dbSNP (classic)	rs1057520844
ClinGen	rs1057520844
ebi	rs1057520844
HLI	rs1057520844
Exac	rs1057520844
Gnomad	rs1057520844
Varsome	rs1057520844
LitVar	rs1057520844
Map	rs1057520844
PheGenI	rs1057520844
Biobank	rs1057520844
1000 genomes	rs1057520844
hgdp	rs1057520844
ensembl	rs1057520844
geneview	rs1057520844
scholar	rs1057520844
google	rs1057520844
pharmgkb	rs1057520844
gwascentral	rs1057520844
openSNP	rs1057520844
23andMe	rs1057520844
SNPshot	rs1057520844
SNPdbe	rs1057520844
MSV3d	rs1057520844
GWAS Ctlg	rs1057520844

Max Magnitude

0

ClinVar
Risk	rs1057520844(A;A)
Alt	rs1057520844(A;A)
Reference	Rs1057520844(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166245220G>A
CLNSRC
CLNACC	RCV000433186.1,