rs80356729

Orientation

plus

Stabilized

plus

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

Make rs80356729(A;A)

Make rs80356729(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

11022413

Gene

TARDBP

is a	snp
is	mentioned by
dbSNP	rs80356729
dbSNP (classic)	rs80356729
ClinGen	rs80356729
ebi	rs80356729
HLI	rs80356729
Exac	rs80356729
Gnomad	rs80356729
Varsome	rs80356729
LitVar	rs80356729
Map	rs80356729
PheGenI	rs80356729
Biobank	rs80356729
1000 genomes	rs80356729
hgdp	rs80356729
ensembl	rs80356729
geneview	rs80356729
scholar	rs80356729
google	rs80356729
pharmgkb	rs80356729
gwascentral	rs80356729
openSNP	rs80356729
23andMe	rs80356729
SNPshot	rs80356729
SNPdbe	rs80356729
MSV3d	rs80356729
GWAS Ctlg	rs80356729

Max Magnitude

0

ClinVar
Risk	rs80356729(A;A)
Alt	rs80356729(A;A)
Reference	Rs80356729(G;G)
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.11022413G>A
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000020655.1,