rs182650126

Orientation

plus

Stabilized

plus

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

Make rs182650126(C;C)

Make rs182650126(C;T)

Reference

GRCh38 38.1/142

Chromosome

2

Position

166280452

Gene	LOC101929680, SCN9A

is a	snp
is	mentioned by
dbSNP	rs182650126
dbSNP (classic)	rs182650126
ClinGen	rs182650126
ebi	rs182650126
HLI	rs182650126
Exac	rs182650126
Gnomad	rs182650126
Varsome	rs182650126
LitVar	rs182650126
Map	rs182650126
PheGenI	rs182650126
Biobank	rs182650126
1000 genomes	rs182650126
hgdp	rs182650126
ensembl	rs182650126
geneview	rs182650126
scholar	rs182650126
google	rs182650126
pharmgkb	rs182650126
gwascentral	rs182650126
openSNP	rs182650126
23andMe	rs182650126
SNPshot	rs182650126
SNPdbe	rs182650126
MSV3d	rs182650126
GWAS Ctlg	rs182650126

Max Magnitude

0

ClinVar
Risk	rs182650126(C;C)
Alt	rs182650126(C;C)
Reference	Rs182650126(T;T)
Significance	Other
Disease	Small fiber neuropathy not specified Inherited Erythromelalgia Paroxysmal extreme pain disorder Familial Febrile Seizures Severe myoclonic epilepsy in infancy Generalized epilepsy with febrile seizures plus Congenital Indifference to Pain not provided Generalized epilepsy with febrile seizures plus Hereditary sensory and autonomic neuropathy type IIA
Variation	info
Gene	LOC101929680 SCN9A
CLNDBN	Small fiber neuropathy not specified Inherited Erythromelalgia Paroxysmal extreme pain disorder Familial Febrile Seizures Severe myoclonic epilepsy in infancy Generalized epilepsy with febrile seizures plus Congenital Indifference to Pain not provided Generalized epilepsy with febrile seizures plus, type 7 Hereditary sensory and autonomic neuropathy type IIA
Reversed	0
HGVS	NC_000002.11:g.167136962T>C
CLNSRC	HGMD OMIM Allelic Variant
CLNACC	RCV000144932.4, RCV000218739.4, RCV000281545.1, RCV000284837.1, RCV000324778.1, RCV000340033.1, RCV000379271.1, RCV000398464.1, RCV000416064.1, RCV000467712.1,