rs121909670

Merged into

rs121909668

Orientation

plus

Stabilized

plus

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

Make rs121909670(C;T)

Make rs121909670(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

31191418

Gene

FUS

is a	snp
is	mentioned by
dbSNP	rs121909670
dbSNP (classic)	rs121909670
ClinGen	rs121909670
ebi	rs121909670
HLI	rs121909670
Exac	rs121909670
Gnomad	rs121909670
Varsome	rs121909670
LitVar	rs121909670
Map	rs121909670
PheGenI	rs121909670
Biobank	rs121909670
1000 genomes	rs121909670
hgdp	rs121909670
ensembl	rs121909670
geneview	rs121909670
scholar	rs121909670
google	rs121909670
pharmgkb	rs121909670
gwascentral	rs121909670
openSNP	rs121909670
23andMe	rs121909670
SNPshot	rs121909670
SNPdbe	rs121909670
MSV3d	rs121909670
GWAS Ctlg	rs121909670

Status

Merged into rs121909668

Max Magnitude

0

OMIM	137070
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121909670(T;T)
Alt	rs121909670(T;T)
Reference	Rs121909670(C;C)
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.31202739C>T
CLNSRC	OMIM Allelic Variant
CLNACC	SCV000037884.1,