rs1057524573

Orientation

plus

Stabilized

plus

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

Make rs1057524573(C;C)

Make rs1057524573(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

165344759

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs1057524573
dbSNP (classic)	rs1057524573
ClinGen	rs1057524573
ebi	rs1057524573
HLI	rs1057524573
Exac	rs1057524573
Gnomad	rs1057524573
Varsome	rs1057524573
LitVar	rs1057524573
Map	rs1057524573
PheGenI	rs1057524573
Biobank	rs1057524573
1000 genomes	rs1057524573
hgdp	rs1057524573
ensembl	rs1057524573
geneview	rs1057524573
scholar	rs1057524573
google	rs1057524573
pharmgkb	rs1057524573
gwascentral	rs1057524573
openSNP	rs1057524573
23andMe	rs1057524573
SNPshot	rs1057524573
SNPdbe	rs1057524573
MSV3d	rs1057524573
GWAS Ctlg	rs1057524573

Max Magnitude

0

ClinVar
Risk	rs1057524573(C;C)
Alt	rs1057524573(C;C)
Reference	Rs1057524573(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166201269T>C
CLNSRC
CLNACC	RCV000431611.1,