rs741810

Orientation

plus

Stabilized

plus

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

Make rs741810(A;A)

Make rs741810(A;C)

Reference

GRCh38 38.1/141

Chromosome

16

Position

31182621

Gene

FUS

is a	snp
is	mentioned by
dbSNP	rs741810
dbSNP (classic)	rs741810
ClinGen	rs741810
ebi	rs741810
HLI	rs741810
Exac	rs741810
Gnomad	rs741810
Varsome	rs741810
LitVar	rs741810
Map	rs741810
PheGenI	rs741810
Biobank	rs741810
1000 genomes	rs741810
hgdp	rs741810
ensembl	rs741810
geneview	rs741810
scholar	rs741810
google	rs741810
pharmgkb	rs741810
gwascentral	rs741810
openSNP	rs741810
23andMe	rs741810
SNPshot	rs741810
SNPdbe	rs741810
MSV3d	rs741810
GWAS Ctlg	rs741810

GMAF

0.2199

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

[PMID 20061612] FUS/TLS genetic variability in sporadic frontotemporal lobar degeneration

ClinVar
Risk	rs741810(A;A) rs741810(G;G)
Alt	rs741810(A;A) rs741810(G;G)
Reference	Rs741810(C;C)
Significance	Non-pathogenic
Disease	not specified Amyotrophic Lateral Sclerosis
Variation	info
Gene	FUS
CLNDBN	not specified Amyotrophic Lateral Sclerosis, Dominant
Reversed	0
HGVS	NC_000016.9:g.31193942C>A
CLNSRC
CLNACC	RCV000251286.1, RCV000356600.1,