rs752076094

Orientation

plus

Stabilized

plus

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

Make rs752076094(A;G)

Make rs752076094(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

31185175

Gene

FUS

is a	snp
is	mentioned by
dbSNP	rs752076094
dbSNP (classic)	rs752076094
ClinGen	rs752076094
ebi	rs752076094
HLI	rs752076094
Exac	rs752076094
Gnomad	rs752076094
Varsome	rs752076094
LitVar	rs752076094
Map	rs752076094
PheGenI	rs752076094
Biobank	rs752076094
1000 genomes	rs752076094
hgdp	rs752076094
ensembl	rs752076094
geneview	rs752076094
scholar	rs752076094
google	rs752076094
pharmgkb	rs752076094
gwascentral	rs752076094
openSNP	rs752076094
23andMe	rs752076094
SNPshot	rs752076094
SNPdbe	rs752076094
MSV3d	rs752076094
GWAS Ctlg	rs752076094

Max Magnitude

0

ClinVar
Risk	rs752076094(G;G)
Alt	rs752076094(G;G)
Reference	Rs752076094(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FUS
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.31196496A>G
CLNSRC
CLNACC	RCV000489255.1,