rs121909668

Orientation

plus

Stabilized

plus

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

Make rs121909668(C;G)

Make rs121909668(G;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

31191418

Gene

FUS

is a	snp
is	mentioned by
dbSNP	rs121909668
dbSNP (classic)	rs121909668
ClinGen	rs121909668
ebi	rs121909668
HLI	rs121909668
Exac	rs121909668
Gnomad	rs121909668
Varsome	rs121909668
LitVar	rs121909668
Map	rs121909668
PheGenI	rs121909668
Biobank	rs121909668
1000 genomes	rs121909668
hgdp	rs121909668
ensembl	rs121909668
geneview	rs121909668
scholar	rs121909668
google	rs121909668
pharmgkb	rs121909668
gwascentral	rs121909668
openSNP	rs121909668
23andMe	rs121909668
SNPshot	rs121909668
SNPdbe	rs121909668
MSV3d	rs121909668
GWAS Ctlg	rs121909668

Merged from

Rs121909670

Max Magnitude

0

OMIM	137070
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121909668(G;G) rs121909668(T;T)
Alt	rs121909668(G;G) rs121909668(T;T)
Reference	Rs121909668(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>G; NC_000016.9:g.31202739C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017609.28, RCV000017611.26,