rs80356730

Orientation

plus

Stabilized

plus

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

Make rs80356730(A;G)

Make rs80356730(G;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

11022418

Gene

TARDBP

is a	snp
is	mentioned by
dbSNP	rs80356730
dbSNP (classic)	rs80356730
ClinGen	rs80356730
ebi	rs80356730
HLI	rs80356730
Exac	rs80356730
Gnomad	rs80356730
Varsome	rs80356730
LitVar	rs80356730
Map	rs80356730
PheGenI	rs80356730
Biobank	rs80356730
1000 genomes	rs80356730
hgdp	rs80356730
ensembl	rs80356730
geneview	rs80356730
scholar	rs80356730
google	rs80356730
pharmgkb	rs80356730
gwascentral	rs80356730
openSNP	rs80356730
23andMe	rs80356730
SNPshot	rs80356730
SNPdbe	rs80356730
MSV3d	rs80356730
GWAS Ctlg	rs80356730

Max Magnitude

0

OMIM	605078
Desc
Variant	0001
Related	also

ClinVar
Risk	rs80356730(G;G)
Alt	rs80356730(G;G)
Reference	Rs80356730(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.11082475A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005539.3,

[PMID 18309045] TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis.