rs797044933

Orientation

minus

Stabilized

minus

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

Make rs797044933(C;T)

Make rs797044933(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

165154514

Gene

SCN3A

is a	snp
is	mentioned by
dbSNP	rs797044933
dbSNP (classic)	rs797044933
ClinGen	rs797044933
ebi	rs797044933
HLI	rs797044933
Exac	rs797044933
Gnomad	rs797044933
Varsome	rs797044933
LitVar	rs797044933
Map	rs797044933
PheGenI	rs797044933
Biobank	rs797044933
1000 genomes	rs797044933
hgdp	rs797044933
ensembl	rs797044933
geneview	rs797044933
scholar	rs797044933
google	rs797044933
pharmgkb	rs797044933
gwascentral	rs797044933
openSNP	rs797044933
23andMe	rs797044933
SNPshot	rs797044933
SNPdbe	rs797044933
MSV3d	rs797044933
GWAS Ctlg	rs797044933

Max Magnitude

0

ClinVar
Risk	rs797044933(T;T)
Alt	rs797044933(T;T)
Reference	Rs797044933(C;C)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	SCN2A SCN3A
CLNDBN	Inborn genetic diseases
Reversed	1
HGVS	NC_000002.11:g.166011024G>A
CLNSRC
CLNACC	RCV000190774.1,