rs121908395

Orientation

plus

Stabilized

plus

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

Make rs121908395(C;C)

Make rs121908395(C;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

11022278

Gene

TARDBP

is a	snp
is	mentioned by
dbSNP	rs121908395
dbSNP (classic)	rs121908395
ClinGen	rs121908395
ebi	rs121908395
HLI	rs121908395
Exac	rs121908395
Gnomad	rs121908395
Varsome	rs121908395
LitVar	rs121908395
Map	rs121908395
PheGenI	rs121908395
Biobank	rs121908395
1000 genomes	rs121908395
hgdp	rs121908395
ensembl	rs121908395
geneview	rs121908395
scholar	rs121908395
google	rs121908395
pharmgkb	rs121908395
gwascentral	rs121908395
openSNP	rs121908395
23andMe	rs121908395
SNPshot	rs121908395
SNPdbe	rs121908395
MSV3d	rs121908395
GWAS Ctlg	rs121908395

Max Magnitude

0

OMIM	605078
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121908395(C;C)
Alt	rs121908395(C;C)
Reference	Rs121908395(G;G)
Significance	Pathogenic
Disease	Amyotrophic lateral sclerosis type 10
Variation	info
Gene	TARDBP
CLNDBN	Amyotrophic lateral sclerosis type 10
Reversed	0
HGVS	NC_000001.10:g.11082335G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005542.4,