rs387907274

Orientation

plus

Stabilized

plus

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

Make rs387907274(C;T)

Make rs387907274(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

31189158

Gene

FUS

is a	snp
is	mentioned by
dbSNP	rs387907274
dbSNP (classic)	rs387907274
ClinGen	rs387907274
ebi	rs387907274
HLI	rs387907274
Exac	rs387907274
Gnomad	rs387907274
Varsome	rs387907274
LitVar	rs387907274
Map	rs387907274
PheGenI	rs387907274
Biobank	rs387907274
1000 genomes	rs387907274
hgdp	rs387907274
ensembl	rs387907274
geneview	rs387907274
scholar	rs387907274
google	rs387907274
pharmgkb	rs387907274
gwascentral	rs387907274
openSNP	rs387907274
23andMe	rs387907274
SNPshot	rs387907274
SNPdbe	rs387907274
MSV3d	rs387907274
GWAS Ctlg	rs387907274

Max Magnitude

0

ClinVar
Risk	rs387907274(T;T)
Alt	rs387907274(T;T)
Reference	Rs387907274(C;C)
Significance	Pathogenic
Disease	Tremor
Variation	info
Gene	FUS
CLNDBN	Tremor, hereditary essential, 4
Reversed	0
HGVS	NC_000016.9:g.31200479C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000030720.28,