rs796053179

Orientation

plus

Stabilized

plus

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

Make rs796053179(C;T)

Make rs796053179(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

165313908

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs796053179
dbSNP (classic)	rs796053179
ClinGen	rs796053179
ebi	rs796053179
HLI	rs796053179
Exac	rs796053179
Gnomad	rs796053179
Varsome	rs796053179
LitVar	rs796053179
Map	rs796053179
PheGenI	rs796053179
Biobank	rs796053179
1000 genomes	rs796053179
hgdp	rs796053179
ensembl	rs796053179
geneview	rs796053179
scholar	rs796053179
google	rs796053179
pharmgkb	rs796053179
gwascentral	rs796053179
openSNP	rs796053179
23andMe	rs796053179
SNPshot	rs796053179
SNPdbe	rs796053179
MSV3d	rs796053179
GWAS Ctlg	rs796053179

Max Magnitude

0

ClinVar
Risk	rs796053179(T;T)
Alt	rs796053179(T;T)
Reference	Rs796053179(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166170418C>T
CLNSRC
CLNACC	RCV000189205.1,