rs1057518094

Orientation

minus

Stabilized

minus

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

Make rs1057518094(A;C)

Make rs1057518094(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

166047707

Gene

SCN1A

is a	snp
is	mentioned by
dbSNP	rs1057518094
dbSNP (classic)	rs1057518094
ClinGen	rs1057518094
ebi	rs1057518094
HLI	rs1057518094
Exac	rs1057518094
Gnomad	rs1057518094
Varsome	rs1057518094
LitVar	rs1057518094
Map	rs1057518094
PheGenI	rs1057518094
Biobank	rs1057518094
1000 genomes	rs1057518094
hgdp	rs1057518094
ensembl	rs1057518094
geneview	rs1057518094
scholar	rs1057518094
google	rs1057518094
pharmgkb	rs1057518094
gwascentral	rs1057518094
openSNP	rs1057518094
23andMe	rs1057518094
SNPshot	rs1057518094
SNPdbe	rs1057518094
MSV3d	rs1057518094
GWAS Ctlg	rs1057518094

Max Magnitude

0

ClinVar
Risk	rs1057518094(C;C)
Alt	rs1057518094(C;C)
Reference	Rs1057518094(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN1A
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.166904217T>G
CLNSRC
CLNACC	RCV000414158.1,