rs1057521767

Orientation

plus

Stabilized

plus

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

Make rs1057521767(A;C)

Make rs1057521767(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

51789410

Gene

SCN8A

is a	snp
is	mentioned by
dbSNP	rs1057521767
dbSNP (classic)	rs1057521767
ClinGen	rs1057521767
ebi	rs1057521767
HLI	rs1057521767
Exac	rs1057521767
Gnomad	rs1057521767
Varsome	rs1057521767
LitVar	rs1057521767
Map	rs1057521767
PheGenI	rs1057521767
Biobank	rs1057521767
1000 genomes	rs1057521767
hgdp	rs1057521767
ensembl	rs1057521767
geneview	rs1057521767
scholar	rs1057521767
google	rs1057521767
pharmgkb	rs1057521767
gwascentral	rs1057521767
openSNP	rs1057521767
23andMe	rs1057521767
SNPshot	rs1057521767
SNPdbe	rs1057521767
MSV3d	rs1057521767
GWAS Ctlg	rs1057521767

Max Magnitude

0

ClinVar
Risk	rs1057521767(C;C)
Alt	rs1057521767(C;C)
Reference	Rs1057521767(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN8A
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.52183194A>C
CLNSRC
CLNACC	RCV000438505.1,