rs1057518356

Orientation

plus

Stabilized

plus

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

Make rs1057518356(C;C)

Make rs1057518356(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

51762665

Gene

SCN8A

is a	snp
is	mentioned by
dbSNP	rs1057518356
dbSNP (classic)	rs1057518356
ClinGen	rs1057518356
ebi	rs1057518356
HLI	rs1057518356
Exac	rs1057518356
Gnomad	rs1057518356
Varsome	rs1057518356
LitVar	rs1057518356
Map	rs1057518356
PheGenI	rs1057518356
Biobank	rs1057518356
1000 genomes	rs1057518356
hgdp	rs1057518356
ensembl	rs1057518356
geneview	rs1057518356
scholar	rs1057518356
google	rs1057518356
pharmgkb	rs1057518356
gwascentral	rs1057518356
openSNP	rs1057518356
23andMe	rs1057518356
SNPshot	rs1057518356
SNPdbe	rs1057518356
MSV3d	rs1057518356
GWAS Ctlg	rs1057518356

Max Magnitude

0

ClinVar
Risk	rs1057518356(C;C)
Alt	rs1057518356(C;C)
Reference	Rs1057518356(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN8A
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.52156449T>C
CLNSRC
CLNACC	RCV000413870.1,