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rs28940285

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs28940285(C;C)
Make rs28940285(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position20645640
GenePINK1, PINK1-AS
is asnp
is mentioned by
dbSNPrs28940285
ebirs28940285
HLIrs28940285
Exacrs28940285
Varsomers28940285
Maprs28940285
PheGenIrs28940285
hapmaprs28940285
1000 genomesrs28940285
hgdprs28940285
ensemblrs28940285
gopubmedrs28940285
geneviewrs28940285
scholarrs28940285
googlers28940285
pharmgkbrs28940285
gwascentralrs28940285
openSNPrs28940285
23andMers28940285
23andMe allrs28940285
SNP Nexus

SNPshotrs28940285
SNPdbers28940285
MSV3drs28940285
GWAS Ctlgrs28940285
Max Magnitude0
OMIM608309
DescPARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET
Variant0005
Relatedalso
ClinVar
Risk rs28940285(C;C)
Alt rs28940285(C;C)
Reference rs28940285(T;T)
Significance Pathogenic
Disease Parkinson disease 6
Variation info
Gene PINK1-AS PINK1
CLNDBN Parkinson disease 6, autosomal recessive early-onset
Reversed 0
HGVS NC_000001.10:g.20972133T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000002509.3,