rs387906627

Orientation

plus

Stabilized

plus

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

Make rs387906627(C;T)

Make rs387906627(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

31191052

Gene

FUS

is a	snp
is	mentioned by
dbSNP	rs387906627
dbSNP (classic)	rs387906627
ClinGen	rs387906627
ebi	rs387906627
HLI	rs387906627
Exac	rs387906627
Gnomad	rs387906627
Varsome	rs387906627
LitVar	rs387906627
Map	rs387906627
PheGenI	rs387906627
Biobank	rs387906627
1000 genomes	rs387906627
hgdp	rs387906627
ensembl	rs387906627
geneview	rs387906627
scholar	rs387906627
google	rs387906627
pharmgkb	rs387906627
gwascentral	rs387906627
openSNP	rs387906627
23andMe	rs387906627
SNPshot	rs387906627
SNPdbe	rs387906627
MSV3d	rs387906627
GWAS Ctlg	rs387906627

Max Magnitude

0

ClinVar
Risk	rs387906627(T;T)
Alt	rs387906627(T;T)
Reference	Rs387906627(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.31202373C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000022556.30,