rs121909671

Orientation

plus

Stabilized

plus

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

Make rs121909671(A;A)

Make rs121909671(A;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

31191419

Gene

FUS

is a	snp
is	mentioned by
dbSNP	rs121909671
dbSNP (classic)	rs121909671
ClinGen	rs121909671
ebi	rs121909671
HLI	rs121909671
Exac	rs121909671
Gnomad	rs121909671
Varsome	rs121909671
LitVar	rs121909671
Map	rs121909671
PheGenI	rs121909671
Biobank	rs121909671
1000 genomes	rs121909671
hgdp	rs121909671
ensembl	rs121909671
geneview	rs121909671
scholar	rs121909671
google	rs121909671
pharmgkb	rs121909671
gwascentral	rs121909671
openSNP	rs121909671
23andMe	rs121909671
SNPshot	rs121909671
SNPdbe	rs121909671
MSV3d	rs121909671
GWAS Ctlg	rs121909671

Max Magnitude

0

OMIM	137070
Desc
Variant	0005
Related	also

ClinVar
Risk	rs121909671(A;A)
Alt	rs121909671(A;A)
Reference	Rs121909671(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.31202740G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017612.28,