rs138404783

Orientation

plus

Stabilized

plus

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

Make rs138404783(A;G)

Make rs138404783(G;G)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38752313

Gene

SCN10A

is a	snp
is	mentioned by
dbSNP	rs138404783
dbSNP (classic)	rs138404783
ClinGen	rs138404783
ebi	rs138404783
HLI	rs138404783
Exac	rs138404783
Gnomad	rs138404783
Varsome	rs138404783
LitVar	rs138404783
Map	rs138404783
PheGenI	rs138404783
Biobank	rs138404783
1000 genomes	rs138404783
hgdp	rs138404783
ensembl	rs138404783
geneview	rs138404783
scholar	rs138404783
google	rs138404783
pharmgkb	rs138404783
gwascentral	rs138404783
openSNP	rs138404783
23andMe	rs138404783
SNPshot	rs138404783
SNPdbe	rs138404783
MSV3d	rs138404783
GWAS Ctlg	rs138404783

Max Magnitude

0

ClinVar
Risk	rs138404783(G;G)
Alt	rs138404783(G;G)
Reference	Rs138404783(A;A)
Significance	Pathogenic
Disease	Episodic pain syndrome not specified
Variation	info
Gene	SCN10A
CLNDBN	Episodic pain syndrome, familial, 2 not specified
Reversed	0
HGVS	NC_000003.11:g.38793804A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000074497.4, RCV000438968.1,