rs28937592

Orientation

plus

Stabilized

plus

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

Make rs28937592(C;T)

Make rs28937592(T;T)

Reference

GRCh38 38.1/141

Chromosome

5

Position

122450708

Gene	MGC32805, SNCAIP

is a	snp
is	mentioned by
dbSNP	rs28937592
dbSNP (classic)	rs28937592
ClinGen	rs28937592
ebi	rs28937592
HLI	rs28937592
Exac	rs28937592
Gnomad	rs28937592
Varsome	rs28937592
LitVar	rs28937592
Map	rs28937592
PheGenI	rs28937592
Biobank	rs28937592
1000 genomes	rs28937592
hgdp	rs28937592
ensembl	rs28937592
geneview	rs28937592
scholar	rs28937592
google	rs28937592
pharmgkb	rs28937592
gwascentral	rs28937592
openSNP	rs28937592
23andMe	rs28937592
SNPshot	rs28937592
SNPdbe	rs28937592
MSV3d	rs28937592
GWAS Ctlg	rs28937592

GMAF

0.001377

Max Magnitude

0

OMIM	603779
Desc	PARKINSON DISEASE
Variant	0001
Related	also

ClinVar
Risk	rs28937592(T;T)
Alt	rs28937592(T;T)
Reference	Rs28937592(C;C)
Significance	Probable-non-pathogenic
Disease	Parkinson disease Parkinson Disease
Variation	info
Gene	SNCAIP MGC32805
CLNDBN	Parkinson disease, late-onset Parkinson Disease, Dominant/Recessive
Reversed	0
HGVS	NC_000005.9:g.121786403C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006451.2, RCV000314385.1,