rs121909669

Orientation

plus

Stabilized

plus

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

Make rs121909669(A;A)

Make rs121909669(A;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

31191410

Gene

FUS

is a	snp
is	mentioned by
dbSNP	rs121909669
dbSNP (classic)	rs121909669
ClinGen	rs121909669
ebi	rs121909669
HLI	rs121909669
Exac	rs121909669
Gnomad	rs121909669
Varsome	rs121909669
LitVar	rs121909669
Map	rs121909669
PheGenI	rs121909669
Biobank	rs121909669
1000 genomes	rs121909669
hgdp	rs121909669
ensembl	rs121909669
geneview	rs121909669
scholar	rs121909669
google	rs121909669
pharmgkb	rs121909669
gwascentral	rs121909669
openSNP	rs121909669
23andMe	rs121909669
SNPshot	rs121909669
SNPdbe	rs121909669
MSV3d	rs121909669
GWAS Ctlg	rs121909669

Max Magnitude

0

OMIM	137070
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121909669(A;A)
Alt	rs121909669(A;A)
Reference	Rs121909669(G;G)
Significance	Pathogenic
Disease	Amyotrophic lateral sclerosis type 6
Variation	info
Gene	FUS
CLNDBN	Amyotrophic lateral sclerosis type 6
Reversed	0
HGVS	NC_000016.9:g.31202731G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017610.28,