rs80356731

Orientation

plus

Stabilized

plus

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

Make rs80356731(A;G)

Make rs80356731(G;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

11022437

Gene

TARDBP

is a	snp
is	mentioned by
dbSNP	rs80356731
dbSNP (classic)	rs80356731
ClinGen	rs80356731
ebi	rs80356731
HLI	rs80356731
Exac	rs80356731
Gnomad	rs80356731
Varsome	rs80356731
LitVar	rs80356731
Map	rs80356731
PheGenI	rs80356731
Biobank	rs80356731
1000 genomes	rs80356731
hgdp	rs80356731
ensembl	rs80356731
geneview	rs80356731
scholar	rs80356731
google	rs80356731
pharmgkb	rs80356731
gwascentral	rs80356731
openSNP	rs80356731
23andMe	rs80356731
SNPshot	rs80356731
SNPdbe	rs80356731
MSV3d	rs80356731
GWAS Ctlg	rs80356731

Max Magnitude

0

OMIM	605078
Desc
Variant	0008
Related	also

ClinVar
Risk	rs80356731(G;G)
Alt	rs80356731(G;G)
Reference	Rs80356731(A;A)
Significance	Pathogenic
Disease	Amyotrophic lateral sclerosis type 10
Variation	info
Gene	TARDBP
CLNDBN	Amyotrophic lateral sclerosis type 10
Reversed	0
HGVS	NC_000001.10:g.11082494A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005546.3,

[PMID 18438952] TDP-43 mutation in familial amyotrophic lateral sclerosis.