rs796053206

Orientation

plus

Stabilized

plus

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

Make rs796053206(GC;TT)

Make rs796053206(TT;TT)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

165310343

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs796053206
dbSNP (classic)	rs796053206
ClinGen	rs796053206
ebi	rs796053206
HLI	rs796053206
Exac	rs796053206
Gnomad	rs796053206
Varsome	rs796053206
LitVar	rs796053206
Map	rs796053206
PheGenI	rs796053206
Biobank	rs796053206
1000 genomes	rs796053206
hgdp	rs796053206
ensembl	rs796053206
geneview	rs796053206
scholar	rs796053206
google	rs796053206
pharmgkb	rs796053206
gwascentral	rs796053206
openSNP	rs796053206
23andMe	rs796053206
SNPshot	rs796053206
SNPdbe	rs796053206
MSV3d	rs796053206
GWAS Ctlg	rs796053206

Max Magnitude

0

ClinVar
Risk	rs796053206(TT;TT)
Alt	rs796053206(TT;TT)
Reference	Rs796053206(GC;GC)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166166853_166166854delGCinsTT
CLNSRC
CLNACC	RCV000189248.1,