rs80356737

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(TAT;TAT)	0	common in clinvar

Make rs80356737(-;A)

Make rs80356737(A;A)

Reference

GRCh38 38.1/141

Chromosome

1

Position

11022530

Gene

TARDBP

is a	snp
is	mentioned by
dbSNP	rs80356737
dbSNP (classic)	rs80356737
ClinGen	rs80356737
ebi	rs80356737
HLI	rs80356737
Exac	rs80356737
Gnomad	rs80356737
Varsome	rs80356737
LitVar	rs80356737
Map	rs80356737
PheGenI	rs80356737
Biobank	rs80356737
1000 genomes	rs80356737
hgdp	rs80356737
ensembl	rs80356737
geneview	rs80356737
scholar	rs80356737
google	rs80356737
pharmgkb	rs80356737
gwascentral	rs80356737
openSNP	rs80356737
23andMe	rs80356737
SNPshot	rs80356737
SNPdbe	rs80356737
MSV3d	rs80356737
GWAS Ctlg	rs80356737

Max Magnitude

0

ClinVar
Risk	rs80356737(A;A)
Alt	rs80356737(A;A)
Reference	Rs80356737(TAT;TAT)
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.11022530dupA
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000020660.1,

[PMID 18931000] Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis.