rs80356718

Orientation

plus

Stabilized

plus

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

Make rs80356718(A;G)

Make rs80356718(G;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

11022209

Gene

TARDBP

is a	snp
is	mentioned by
dbSNP	rs80356718
dbSNP (classic)	rs80356718
ClinGen	rs80356718
ebi	rs80356718
HLI	rs80356718
Exac	rs80356718
Gnomad	rs80356718
Varsome	rs80356718
LitVar	rs80356718
Map	rs80356718
PheGenI	rs80356718
Biobank	rs80356718
1000 genomes	rs80356718
hgdp	rs80356718
ensembl	rs80356718
geneview	rs80356718
scholar	rs80356718
google	rs80356718
pharmgkb	rs80356718
gwascentral	rs80356718
openSNP	rs80356718
23andMe	rs80356718
SNPshot	rs80356718
SNPdbe	rs80356718
MSV3d	rs80356718
GWAS Ctlg	rs80356718

GMAF

0.0004591

Max Magnitude

0

ClinVar
Risk	rs80356718(G;G)
Alt	rs80356718(G;G)
Reference	Rs80356718(A;A)
Significance	Pathogenic
Disease	Amyotrophic lateral sclerosis type 10
Variation	info
Gene	TARDBP
CLNDBN	Amyotrophic lateral sclerosis type 10
Reversed	0
HGVS	NC_000001.11:g.11022209A>G
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000020671.1,