rs1057518658

Orientation

plus

Stabilized

plus

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

Make rs1057518658(-;-)

Make rs1057518658(-;AC)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

165331409

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs1057518658
dbSNP (classic)	rs1057518658
ClinGen	rs1057518658
ebi	rs1057518658
HLI	rs1057518658
Exac	rs1057518658
Gnomad	rs1057518658
Varsome	rs1057518658
LitVar	rs1057518658
Map	rs1057518658
PheGenI	rs1057518658
Biobank	rs1057518658
1000 genomes	rs1057518658
hgdp	rs1057518658
ensembl	rs1057518658
geneview	rs1057518658
scholar	rs1057518658
google	rs1057518658
pharmgkb	rs1057518658
gwascentral	rs1057518658
openSNP	rs1057518658
23andMe	rs1057518658
SNPshot	rs1057518658
SNPdbe	rs1057518658
MSV3d	rs1057518658
GWAS Ctlg	rs1057518658

Max Magnitude

0

ClinVar
Risk	rs1057518658(-;-)
Alt	rs1057518658(-;-)
Reference	Rs1057518658(AC;AC)
Significance	Pathogenic
Disease	Autism
Variation	info
Gene	SCN2A
CLNDBN	Autism
Reversed	0
HGVS	NC_000002.11:g.166187919_166187920delAC
CLNSRC
CLNACC	RCV000414894.1,