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rs28937592

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs28937592(C;T)
Make rs28937592(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position122450708
GeneMGC32805, SNCAIP
is asnp
is mentioned by
dbSNPrs28937592
ebirs28937592
HLIrs28937592
Exacrs28937592
Varsomers28937592
Maprs28937592
PheGenIrs28937592
hapmaprs28937592
1000 genomesrs28937592
hgdprs28937592
ensemblrs28937592
gopubmedrs28937592
geneviewrs28937592
scholarrs28937592
googlers28937592
pharmgkbrs28937592
gwascentralrs28937592
openSNPrs28937592
23andMers28937592
23andMe allrs28937592
SNP Nexus

SNPshotrs28937592
SNPdbers28937592
MSV3drs28937592
GWAS Ctlgrs28937592
GMAF0.001377
Max Magnitude0
OMIM603779
DescPARKINSON DISEASE
Variant0001
Relatedalso


ClinVar
Risk rs28937592(T;T)
Alt rs28937592(T;T)
Reference rs28937592(C;C)
Significance Unknown
Disease Parkinson disease
Variation info
Gene SNCAIP MGC32805
CLNDBN Parkinson disease, late-onset
Reversed 0
HGVS NC_000005.9:g.121786403C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006451.2,