rs267606832

Orientation

plus

Stabilized

plus

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

Make rs267606832(C;T)

Make rs267606832(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

31185061

Gene

FUS

is a	snp
is	mentioned by
dbSNP	rs267606832
dbSNP (classic)	rs267606832
ClinGen	rs267606832
ebi	rs267606832
HLI	rs267606832
Exac	rs267606832
Gnomad	rs267606832
Varsome	rs267606832
LitVar	rs267606832
Map	rs267606832
PheGenI	rs267606832
Biobank	rs267606832
1000 genomes	rs267606832
hgdp	rs267606832
ensembl	rs267606832
geneview	rs267606832
scholar	rs267606832
google	rs267606832
pharmgkb	rs267606832
gwascentral	rs267606832
openSNP	rs267606832
23andMe	rs267606832
SNPshot	rs267606832
SNPdbe	rs267606832
MSV3d	rs267606832
GWAS Ctlg	rs267606832

Max Magnitude

0

ClinVar
Risk	rs267606832(T;T)
Alt	rs267606832(T;T)
Reference	Rs267606832(C;C)
Significance	Pathogenic
Disease	Amyotrophic lateral sclerosis type 6 Tremor
Variation	info
Gene	FUS
CLNDBN	Amyotrophic lateral sclerosis type 6 Tremor, hereditary essential, 4
Reversed	0
HGVS	NC_000016.9:g.31196382C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017614.28, RCV000030719.24,