rs775214722

Orientation

plus

Stabilized

plus

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

Make rs775214722(A;G)

Make rs775214722(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

166037845

Gene

SCN1A

is a	snp
is	mentioned by
dbSNP	rs775214722
dbSNP (classic)	rs775214722
ClinGen	rs775214722
ebi	rs775214722
HLI	rs775214722
Exac	rs775214722
Gnomad	rs775214722
Varsome	rs775214722
LitVar	rs775214722
Map	rs775214722
PheGenI	rs775214722
Biobank	rs775214722
1000 genomes	rs775214722
hgdp	rs775214722
ensembl	rs775214722
geneview	rs775214722
scholar	rs775214722
google	rs775214722
pharmgkb	rs775214722
gwascentral	rs775214722
openSNP	rs775214722
23andMe	rs775214722
SNPshot	rs775214722
SNPdbe	rs775214722
MSV3d	rs775214722
GWAS Ctlg	rs775214722

Max Magnitude

0

ClinVar
Risk	rs775214722(G;G) rs775214722(T;T)
Alt	rs775214722(G;G) rs775214722(T;T)
Reference	Rs775214722(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SCN1A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166894355A>T
CLNSRC
CLNACC	RCV000188901.1,