rs797044594

Orientation

plus

Stabilized

plus

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

Make rs797044594(C;C)

Make rs797044594(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

11022559

Gene

TARDBP

is a	snp
is	mentioned by
dbSNP	rs797044594
dbSNP (classic)	rs797044594
ClinGen	rs797044594
ebi	rs797044594
HLI	rs797044594
Exac	rs797044594
Gnomad	rs797044594
Varsome	rs797044594
LitVar	rs797044594
Map	rs797044594
PheGenI	rs797044594
Biobank	rs797044594
1000 genomes	rs797044594
hgdp	rs797044594
ensembl	rs797044594
geneview	rs797044594
scholar	rs797044594
google	rs797044594
pharmgkb	rs797044594
gwascentral	rs797044594
openSNP	rs797044594
23andMe	rs797044594
SNPshot	rs797044594
SNPdbe	rs797044594
MSV3d	rs797044594
GWAS Ctlg	rs797044594

Max Magnitude

0

ClinVar
Risk	rs797044594(C;C)
Alt	rs797044594(C;C)
Reference	Rs797044594(G;G)
Significance	Pathogenic
Disease	Amyotrophic lateral sclerosis type 10
Variation	info
Gene	TARDBP
CLNDBN	Amyotrophic lateral sclerosis type 10
Reversed	0
HGVS	NC_000001.10:g.11082616G>C
CLNSRC
CLNACC	RCV000192195.1,