rs80356716

Orientation

plus

Stabilized

plus

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

Make rs80356716(A;A)

Make rs80356716(A;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

11013922

Gene

TARDBP

is a	snp
is	mentioned by
dbSNP	rs80356716
dbSNP (classic)	rs80356716
ClinGen	rs80356716
ebi	rs80356716
HLI	rs80356716
Exac	rs80356716
Gnomad	rs80356716
Varsome	rs80356716
LitVar	rs80356716
Map	rs80356716
PheGenI	rs80356716
Biobank	rs80356716
1000 genomes	rs80356716
hgdp	rs80356716
ensembl	rs80356716
geneview	rs80356716
scholar	rs80356716
google	rs80356716
pharmgkb	rs80356716
gwascentral	rs80356716
openSNP	rs80356716
23andMe	rs80356716
SNPshot	rs80356716
SNPdbe	rs80356716
MSV3d	rs80356716
GWAS Ctlg	rs80356716

Max Magnitude

0

ClinVar
Risk	rs80356716(A;A)
Alt	rs80356716(A;A)
Reference	Rs80356716(T;T)
Significance	Non-pathogenic
Disease	Amyotrophic lateral sclerosis type 10
Variation	info
Gene	TARDBP
CLNDBN	Amyotrophic lateral sclerosis type 10
Reversed	0
HGVS	NC_000001.11:g.11013922T>A
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000020669.1,

[PMID 18545701] TDP-43 is not a common cause of sporadic amyotrophic lateral sclerosis.