rs483352921

Orientation

minus

Stabilized

minus

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

Make rs483352921(C;G)

Make rs483352921(G;G)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38894945

Gene

SCN11A

is a	snp
is	mentioned by
dbSNP	rs483352921
dbSNP (classic)	rs483352921
ClinGen	rs483352921
ebi	rs483352921
HLI	rs483352921
Exac	rs483352921
Gnomad	rs483352921
Varsome	rs483352921
LitVar	rs483352921
Map	rs483352921
PheGenI	rs483352921
Biobank	rs483352921
1000 genomes	rs483352921
hgdp	rs483352921
ensembl	rs483352921
geneview	rs483352921
scholar	rs483352921
google	rs483352921
pharmgkb	rs483352921
gwascentral	rs483352921
openSNP	rs483352921
23andMe	rs483352921
SNPshot	rs483352921
SNPdbe	rs483352921
MSV3d	rs483352921
GWAS Ctlg	rs483352921

Max Magnitude

0

ClinVar
Risk	rs483352921(G;G)
Alt	rs483352921(G;G)
Reference	Rs483352921(C;C)
Significance	Pathogenic
Disease	Episodic pain syndrome
Variation	info
Gene	SCN11A
CLNDBN	Episodic pain syndrome, familial, 3
Reversed	1
HGVS	NC_000003.11:g.38936436G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000074496.3,