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rs74315361

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs74315361(C;C)
Make rs74315361(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position20649034
GenePINK1, PINK1-AS
is asnp
is mentioned by
dbSNPrs74315361
ebirs74315361
HLIrs74315361
Exacrs74315361
Varsomers74315361
Maprs74315361
PheGenIrs74315361
hapmaprs74315361
1000 genomesrs74315361
hgdprs74315361
ensemblrs74315361
gopubmedrs74315361
geneviewrs74315361
scholarrs74315361
googlers74315361
pharmgkbrs74315361
gwascentralrs74315361
openSNPrs74315361
23andMers74315361
23andMe allrs74315361
SNP Nexus

SNPshotrs74315361
SNPdbers74315361
MSV3drs74315361
GWAS Ctlgrs74315361
Max Magnitude0
OMIM608309
Desc
Variant0013
Relatedalso
ClinVar
Risk rs74315361(C;C)
Alt rs74315361(C;C)
Reference rs74315361(T;T)
Significance Other
Disease Parkinson disease 6
Variation info
Gene PINK1-AS PINK1
CLNDBN Parkinson disease 6
Reversed 0
HGVS NC_000001.10:g.20975527T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000002517.4,