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rs74315358

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs74315358(A;A)
Make rs74315358(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position20644549
GenePINK1, PINK1-AS
is asnp
is mentioned by
dbSNPrs74315358
ebirs74315358
HLIrs74315358
Exacrs74315358
Varsomers74315358
Maprs74315358
PheGenIrs74315358
hapmaprs74315358
1000 genomesrs74315358
hgdprs74315358
ensemblrs74315358
gopubmedrs74315358
geneviewrs74315358
scholarrs74315358
googlers74315358
pharmgkbrs74315358
gwascentralrs74315358
openSNPrs74315358
23andMers74315358
23andMe allrs74315358
SNP Nexus

SNPshotrs74315358
SNPdbers74315358
MSV3drs74315358
GWAS Ctlgrs74315358
Max Magnitude0
OMIM608309
Desc
Variant0008
Relatedalso
ClinVar
Risk rs74315358(A;A)
Alt rs74315358(A;A)
Reference rs74315358(G;G)
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.20971042G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002512.2,