rs1057518111

Orientation

plus

Stabilized

plus

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

Make rs1057518111(C;C)

Make rs1057518111(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

165386974

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs1057518111
dbSNP (classic)	rs1057518111
ClinGen	rs1057518111
ebi	rs1057518111
HLI	rs1057518111
Exac	rs1057518111
Gnomad	rs1057518111
Varsome	rs1057518111
LitVar	rs1057518111
Map	rs1057518111
PheGenI	rs1057518111
Biobank	rs1057518111
1000 genomes	rs1057518111
hgdp	rs1057518111
ensembl	rs1057518111
geneview	rs1057518111
scholar	rs1057518111
google	rs1057518111
pharmgkb	rs1057518111
gwascentral	rs1057518111
openSNP	rs1057518111
23andMe	rs1057518111
SNPshot	rs1057518111
SNPdbe	rs1057518111
MSV3d	rs1057518111
GWAS Ctlg	rs1057518111

Max Magnitude

0

ClinVar
Risk	rs1057518111(C;C)
Alt	rs1057518111(C;C)
Reference	Rs1057518111(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166243484T>C
CLNSRC
CLNACC	RCV000414096.1,