rs786205635

Orientation

plus

Stabilized

plus

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

Make rs786205635(-;-)

Make rs786205635(-;CTTA)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

165323158

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs786205635
dbSNP (classic)	rs786205635
ClinGen	rs786205635
ebi	rs786205635
HLI	rs786205635
Exac	rs786205635
Gnomad	rs786205635
Varsome	rs786205635
LitVar	rs786205635
Map	rs786205635
PheGenI	rs786205635
Biobank	rs786205635
1000 genomes	rs786205635
hgdp	rs786205635
ensembl	rs786205635
geneview	rs786205635
scholar	rs786205635
google	rs786205635
pharmgkb	rs786205635
gwascentral	rs786205635
openSNP	rs786205635
23andMe	rs786205635
SNPshot	rs786205635
SNPdbe	rs786205635
MSV3d	rs786205635
GWAS Ctlg	rs786205635

Max Magnitude

0

ClinVar
Risk	rs786205635(-;-)
Alt	rs786205635(-;-)
Reference	Rs786205635(CTTA;CTTA)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166179668_166179671delCTTA
CLNSRC
CLNACC	RCV000171497.1,