rs1052352

Orientation

plus

Stabilized

plus

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

Make rs1052352(C;T)

Make rs1052352(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

31183958

Gene

FUS

is a	snp
is	mentioned by
dbSNP	rs1052352
dbSNP (classic)	rs1052352
ClinGen	rs1052352
ebi	rs1052352
HLI	rs1052352
Exac	rs1052352
Gnomad	rs1052352
Varsome	rs1052352
LitVar	rs1052352
Map	rs1052352
PheGenI	rs1052352
Biobank	rs1052352
1000 genomes	rs1052352
hgdp	rs1052352
ensembl	rs1052352
geneview	rs1052352
scholar	rs1052352
google	rs1052352
pharmgkb	rs1052352
gwascentral	rs1052352
openSNP	rs1052352
23andMe	rs1052352
SNPshot	rs1052352
SNPdbe	rs1052352
MSV3d	rs1052352
GWAS Ctlg	rs1052352

GMAF

0.4646

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

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

ClinVar
Risk	rs1052352(T;T)
Alt	rs1052352(T;T)
Reference	Rs1052352(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.31195279C>T
CLNSRC
CLNACC	RCV000244413.1, RCV000277026.1,