rs80356743

Orientation

plus

Stabilized

plus

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

Make rs80356743(C;T)

Make rs80356743(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

11022587

Gene

TARDBP

is a	snp
is	mentioned by
dbSNP	rs80356743
dbSNP (classic)	rs80356743
ClinGen	rs80356743
ebi	rs80356743
HLI	rs80356743
Exac	rs80356743
Gnomad	rs80356743
Varsome	rs80356743
LitVar	rs80356743
Map	rs80356743
PheGenI	rs80356743
Biobank	rs80356743
1000 genomes	rs80356743
hgdp	rs80356743
ensembl	rs80356743
geneview	rs80356743
scholar	rs80356743
google	rs80356743
pharmgkb	rs80356743
gwascentral	rs80356743
openSNP	rs80356743
23andMe	rs80356743
SNPshot	rs80356743
SNPdbe	rs80356743
MSV3d	rs80356743
GWAS Ctlg	rs80356743

Max Magnitude

0

ClinVar
Risk	rs80356743(T;T)
Alt	rs80356743(T;T)
Reference	Rs80356743(C;C)
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.11022587C>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000020668.1,

[PMID 19224587] High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosis.