rs606231280

Orientation

minus

Stabilized

minus

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

Make rs606231280(C;C)

Make rs606231280(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

38909154

Gene

SCN11A

is a	snp
is	mentioned by
dbSNP	rs606231280
dbSNP (classic)	rs606231280
ClinGen	rs606231280
ebi	rs606231280
HLI	rs606231280
Exac	rs606231280
Gnomad	rs606231280
Varsome	rs606231280
LitVar	rs606231280
Map	rs606231280
PheGenI	rs606231280
Biobank	rs606231280
1000 genomes	rs606231280
hgdp	rs606231280
ensembl	rs606231280
geneview	rs606231280
scholar	rs606231280
google	rs606231280
pharmgkb	rs606231280
gwascentral	rs606231280
openSNP	rs606231280
23andMe	rs606231280
SNPshot	rs606231280
SNPdbe	rs606231280
MSV3d	rs606231280
GWAS Ctlg	rs606231280

Max Magnitude

0

ClinVar
Risk	rs606231280(C;C)
Alt	rs606231280(C;C)
Reference	Rs606231280(T;T)
Significance	Pathogenic
Disease	Episodic pain syndrome
Variation	info
Gene	SCN11A
CLNDBN	Episodic pain syndrome, familial, 3
Reversed	1
HGVS	NC_000003.11:g.38950645A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000144935.3,