rs138607170

Orientation

plus

Stabilized

plus

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

Make rs138607170(A;A)

Make rs138607170(A;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

38925454

Gene

SCN11A

is a	snp
is	mentioned by
dbSNP	rs138607170
dbSNP (classic)	rs138607170
ClinGen	rs138607170
ebi	rs138607170
HLI	rs138607170
Exac	rs138607170
Gnomad	rs138607170
Varsome	rs138607170
LitVar	rs138607170
Map	rs138607170
PheGenI	rs138607170
Biobank	rs138607170
1000 genomes	rs138607170
hgdp	rs138607170
ensembl	rs138607170
geneview	rs138607170
scholar	rs138607170
google	rs138607170
pharmgkb	rs138607170
gwascentral	rs138607170
openSNP	rs138607170
23andMe	rs138607170
SNPshot	rs138607170
SNPdbe	rs138607170
MSV3d	rs138607170
GWAS Ctlg	rs138607170

Max Magnitude

0

ClinVar
Risk	rs138607170(A;A)
Alt	rs138607170(A;A)
Reference	Rs138607170(G;G)
Significance	Pathogenic
Disease	Episodic pain syndrome
Variation	info
Gene	SCN11A
CLNDBN	Episodic pain syndrome, familial, 3
Reversed	0
HGVS	NC_000003.11:g.38966945G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000074495.3,