rs55774500

Orientation

minus

Stabilized

minus

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

Make rs55774500(A;A)

Make rs55774500(A;C)

Reference

GRCh38 38.1/142

Chromosome

6

Position

162262692

Gene

PARK2

is a	snp
is	mentioned by
dbSNP	rs55774500
dbSNP (classic)	rs55774500
ClinGen	rs55774500
ebi	rs55774500
HLI	rs55774500
Exac	rs55774500
Gnomad	rs55774500
Varsome	rs55774500
LitVar	rs55774500
Map	rs55774500
PheGenI	rs55774500
Biobank	rs55774500
1000 genomes	rs55774500
hgdp	rs55774500
ensembl	rs55774500
geneview	rs55774500
scholar	rs55774500
google	rs55774500
pharmgkb	rs55774500
gwascentral	rs55774500
openSNP	rs55774500
23andMe	rs55774500
SNPshot	rs55774500
SNPdbe	rs55774500
MSV3d	rs55774500
GWAS Ctlg	rs55774500

GMAF

0.001377

Max Magnitude

0

OMIM	602544
Desc
Variant	0011
Related	also

ClinVar
Risk	rs55774500(A;A) rs55774500(T;T)
Alt	rs55774500(A;A) rs55774500(T;T)
Reference	Rs55774500(C;C)
Significance	Other
Disease	Parkinson disease 2 not specified
Variation	info
Gene	PARK2
CLNDBN	Parkinson disease 2 not specified
Reversed	1
HGVS	NC_000006.11:g.162683724G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007454.7, RCV000455485.1,