rs773824421

Orientation

plus

Stabilized

plus

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

Make rs773824421(G;G)

Make rs773824421(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

166294664

Gene	LOC101929680, SCN9A

is a	snp
is	mentioned by
dbSNP	rs773824421
dbSNP (classic)	rs773824421
ClinGen	rs773824421
ebi	rs773824421
HLI	rs773824421
Exac	rs773824421
Gnomad	rs773824421
Varsome	rs773824421
LitVar	rs773824421
Map	rs773824421
PheGenI	rs773824421
Biobank	rs773824421
1000 genomes	rs773824421
hgdp	rs773824421
ensembl	rs773824421
geneview	rs773824421
scholar	rs773824421
google	rs773824421
pharmgkb	rs773824421
gwascentral	rs773824421
openSNP	rs773824421
23andMe	rs773824421
SNPshot	rs773824421
SNPdbe	rs773824421
MSV3d	rs773824421
GWAS Ctlg	rs773824421

Max Magnitude

0

ClinVar
Risk	rs773824421(G;G)
Alt	rs773824421(G;G)
Reference	Rs773824421(T;T)
Significance	Probable-Pathogenic
Disease	Generalized epilepsy with febrile seizures plus
Variation	info
Gene	LOC101929680 SCN9A
CLNDBN	Generalized epilepsy with febrile seizures plus, type 7
Reversed	0
HGVS	NC_000002.11:g.167151174T>G
CLNSRC
CLNACC	RCV000462867.1,