rs80356727

Orientation

plus

Stabilized

plus

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

Make rs80356727(A;A)

Make rs80356727(A;C)

Reference

GRCh38 38.1/141

Chromosome

1

Position

11022400

Gene

TARDBP

is a	snp
is	mentioned by
dbSNP	rs80356727
dbSNP (classic)	rs80356727
ClinGen	rs80356727
ebi	rs80356727
HLI	rs80356727
Exac	rs80356727
Gnomad	rs80356727
Varsome	rs80356727
LitVar	rs80356727
Map	rs80356727
PheGenI	rs80356727
Biobank	rs80356727
1000 genomes	rs80356727
hgdp	rs80356727
ensembl	rs80356727
geneview	rs80356727
scholar	rs80356727
google	rs80356727
pharmgkb	rs80356727
gwascentral	rs80356727
openSNP	rs80356727
23andMe	rs80356727
SNPshot	rs80356727
SNPdbe	rs80356727
MSV3d	rs80356727
GWAS Ctlg	rs80356727

Max Magnitude

0

OMIM	605078
Desc
Variant	0002
Related	also

ClinVar
Risk	rs80356727(A;A)
Alt	rs80356727(A;A)
Reference	Rs80356727(C;C)
Significance	Pathogenic
Disease	Amyotrophic lateral sclerosis type 10
Variation	info
Gene	TARDBP
CLNDBN	Amyotrophic lateral sclerosis type 10
Reversed	0
HGVS	NC_000001.10:g.11082457C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005540.4,