rs80356728

Orientation

plus

Stabilized

plus

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

Make rs80356728(A;A)

Make rs80356728(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

11022404

Gene

TARDBP

is a	snp
is	mentioned by
dbSNP	rs80356728
dbSNP (classic)	rs80356728
ClinGen	rs80356728
ebi	rs80356728
HLI	rs80356728
Exac	rs80356728
Gnomad	rs80356728
Varsome	rs80356728
LitVar	rs80356728
Map	rs80356728
PheGenI	rs80356728
Biobank	rs80356728
1000 genomes	rs80356728
hgdp	rs80356728
ensembl	rs80356728
geneview	rs80356728
scholar	rs80356728
google	rs80356728
pharmgkb	rs80356728
gwascentral	rs80356728
openSNP	rs80356728
23andMe	rs80356728
SNPshot	rs80356728
SNPdbe	rs80356728
MSV3d	rs80356728
GWAS Ctlg	rs80356728

Max Magnitude

0

ClinVar
Risk	rs80356728(A;A)
Alt	rs80356728(A;A)
Reference	Rs80356728(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.11022404G>A
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000020677.1,