rs80356741

Orientation

plus

Stabilized

plus

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

Make rs80356741(A;G)

Make rs80356741(G;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

11022577

Gene

TARDBP

is a	snp
is	mentioned by
dbSNP	rs80356741
dbSNP (classic)	rs80356741
ClinGen	rs80356741
ebi	rs80356741
HLI	rs80356741
Exac	rs80356741
Gnomad	rs80356741
Varsome	rs80356741
LitVar	rs80356741
Map	rs80356741
PheGenI	rs80356741
Biobank	rs80356741
1000 genomes	rs80356741
hgdp	rs80356741
ensembl	rs80356741
geneview	rs80356741
scholar	rs80356741
google	rs80356741
pharmgkb	rs80356741
gwascentral	rs80356741
openSNP	rs80356741
23andMe	rs80356741
SNPshot	rs80356741
SNPdbe	rs80356741
MSV3d	rs80356741
GWAS Ctlg	rs80356741

Max Magnitude

0

ClinVar
Risk	rs80356741(G;G)
Alt	rs80356741(G;G)
Reference	Rs80356741(A;A)
Significance	Pathogenic
Disease	Amyotrophic lateral sclerosis type 10
Variation	info
Gene	TARDBP
CLNDBN	Amyotrophic lateral sclerosis type 10
Reversed	0
HGVS	NC_000001.11:g.11022577A>G
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000020666.1,