rs267606833

Orientation

plus

Stabilized

plus

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

Make rs267606833(A;T)

Make rs267606833(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

31191427

Gene

FUS

is a	snp
is	mentioned by
dbSNP	rs267606833
dbSNP (classic)	rs267606833
ClinGen	rs267606833
ebi	rs267606833
HLI	rs267606833
Exac	rs267606833
Gnomad	rs267606833
Varsome	rs267606833
LitVar	rs267606833
Map	rs267606833
PheGenI	rs267606833
Biobank	rs267606833
1000 genomes	rs267606833
hgdp	rs267606833
ensembl	rs267606833
geneview	rs267606833
scholar	rs267606833
google	rs267606833
pharmgkb	rs267606833
gwascentral	rs267606833
openSNP	rs267606833
23andMe	rs267606833
SNPshot	rs267606833
SNPdbe	rs267606833
MSV3d	rs267606833
GWAS Ctlg	rs267606833

Max Magnitude

0

ClinVar
Risk	rs267606833(T;T)
Alt	rs267606833(T;T)
Reference	Rs267606833(A;A)
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.31202748A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017615.28,