rs387906628

Orientation

plus

Stabilized

plus

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

Make rs387906628(A;A)

Make rs387906628(A;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

31185031

Gene

FUS

is a	snp
is	mentioned by
dbSNP	rs387906628
dbSNP (classic)	rs387906628
ClinGen	rs387906628
ebi	rs387906628
HLI	rs387906628
Exac	rs387906628
Gnomad	rs387906628
Varsome	rs387906628
LitVar	rs387906628
Map	rs387906628
PheGenI	rs387906628
Biobank	rs387906628
1000 genomes	rs387906628
hgdp	rs387906628
ensembl	rs387906628
geneview	rs387906628
scholar	rs387906628
google	rs387906628
pharmgkb	rs387906628
gwascentral	rs387906628
openSNP	rs387906628
23andMe	rs387906628
SNPshot	rs387906628
SNPdbe	rs387906628
MSV3d	rs387906628
GWAS Ctlg	rs387906628

Max Magnitude

0

ClinVar
Risk	rs387906628(A;A)
Alt	rs387906628(A;A)
Reference	Rs387906628(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.31196352G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000022557.30,