rs797044985

Orientation

minus

Stabilized

minus

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

Make rs797044985(G;G)

Make rs797044985(G;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

166037774

Gene

SCN1A

is a	snp
is	mentioned by
dbSNP	rs797044985
dbSNP (classic)	rs797044985
ClinGen	rs797044985
ebi	rs797044985
HLI	rs797044985
Exac	rs797044985
Gnomad	rs797044985
Varsome	rs797044985
LitVar	rs797044985
Map	rs797044985
PheGenI	rs797044985
Biobank	rs797044985
1000 genomes	rs797044985
hgdp	rs797044985
ensembl	rs797044985
geneview	rs797044985
scholar	rs797044985
google	rs797044985
pharmgkb	rs797044985
gwascentral	rs797044985
openSNP	rs797044985
23andMe	rs797044985
SNPshot	rs797044985
SNPdbe	rs797044985
MSV3d	rs797044985
GWAS Ctlg	rs797044985

Max Magnitude

0

ClinVar
Risk	rs797044985(G;G)
Alt	rs797044985(G;G)
Reference	Rs797044985(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SCN1A
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.166894284A>C
CLNSRC
CLNACC	RCV000190449.1,