rs80356732

Orientation

plus

Stabilized

plus

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

Make rs80356732(A;A)

Make rs80356732(A;C)

Reference

GRCh38 38.1/141

Chromosome

1

Position

11022444

Gene

TARDBP

is a	snp
is	mentioned by
dbSNP	rs80356732
dbSNP (classic)	rs80356732
ClinGen	rs80356732
ebi	rs80356732
HLI	rs80356732
Exac	rs80356732
Gnomad	rs80356732
Varsome	rs80356732
LitVar	rs80356732
Map	rs80356732
PheGenI	rs80356732
Biobank	rs80356732
1000 genomes	rs80356732
hgdp	rs80356732
ensembl	rs80356732
geneview	rs80356732
scholar	rs80356732
google	rs80356732
pharmgkb	rs80356732
gwascentral	rs80356732
openSNP	rs80356732
23andMe	rs80356732
SNPshot	rs80356732
SNPdbe	rs80356732
MSV3d	rs80356732
GWAS Ctlg	rs80356732

Max Magnitude

0

ClinVar
Risk	rs80356732(A;A)
Alt	rs80356732(A;A)
Reference	Rs80356732(C;C)
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.11022444C>A
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000020656.1,