rs730880272

Orientation

plus

Stabilized

plus

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

Make rs730880272(G;T)

Make rs730880272(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

22

Position

32493282

Gene

FBXO7

is a	snp
is	mentioned by
dbSNP	rs730880272
dbSNP (classic)	rs730880272
ClinGen	rs730880272
ebi	rs730880272
HLI	rs730880272
Exac	rs730880272
Gnomad	rs730880272
Varsome	rs730880272
LitVar	rs730880272
Map	rs730880272
PheGenI	rs730880272
Biobank	rs730880272
1000 genomes	rs730880272
hgdp	rs730880272
ensembl	rs730880272
geneview	rs730880272
scholar	rs730880272
google	rs730880272
pharmgkb	rs730880272
gwascentral	rs730880272
openSNP	rs730880272
23andMe	rs730880272
SNPshot	rs730880272
SNPdbe	rs730880272
MSV3d	rs730880272
GWAS Ctlg	rs730880272

Max Magnitude

0

ClinVar
Risk	rs730880272(T;T)
Alt	rs730880272(T;T)
Reference	Rs730880272(G;G)
Significance	Pathogenic
Disease	Parkinson disease 15
Variation	info
Gene	FBXO7
CLNDBN	Parkinson disease 15
Reversed	0
HGVS	NC_000022.10:g.32889269G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005079.3,