rs1057519010

Orientation

plus

Stabilized

plus

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

Make rs1057519010(-;-)

Make rs1057519010(-;GGAGTGAATCTCT)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

165374775

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs1057519010
dbSNP (classic)	rs1057519010
ClinGen	rs1057519010
ebi	rs1057519010
HLI	rs1057519010
Exac	rs1057519010
Gnomad	rs1057519010
Varsome	rs1057519010
LitVar	rs1057519010
Map	rs1057519010
PheGenI	rs1057519010
Biobank	rs1057519010
1000 genomes	rs1057519010
hgdp	rs1057519010
ensembl	rs1057519010
geneview	rs1057519010
scholar	rs1057519010
google	rs1057519010
pharmgkb	rs1057519010
gwascentral	rs1057519010
openSNP	rs1057519010
23andMe	rs1057519010
SNPshot	rs1057519010
SNPdbe	rs1057519010
MSV3d	rs1057519010
GWAS Ctlg	rs1057519010

Max Magnitude

0

ClinVar
Risk	rs1057519010(-;-)
Alt	rs1057519010(-;-)
Reference	Rs1057519010(GGAGTGAATCTCT;GGAGTGAATCTCT)
Significance	Probable-Pathogenic
Disease	intellectual deficiency
Variation	info
Gene	SCN2A
CLNDBN	intellectual deficiency
Reversed	0
HGVS	NC_000002.11:g.166231285_166231297delGGAGTGAATCTCT
CLNSRC
CLNACC	RCV000415077.1,