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rs74315356

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs74315356(A;A)
Make rs74315356(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position20649054
GenePINK1, PINK1-AS
is asnp
is mentioned by
dbSNPrs74315356
ebirs74315356
HLIrs74315356
Exacrs74315356
Varsomers74315356
Maprs74315356
PheGenIrs74315356
hapmaprs74315356
1000 genomesrs74315356
hgdprs74315356
ensemblrs74315356
gopubmedrs74315356
geneviewrs74315356
scholarrs74315356
googlers74315356
pharmgkbrs74315356
gwascentralrs74315356
openSNPrs74315356
23andMers74315356
23andMe allrs74315356
SNP Nexus

SNPshotrs74315356
SNPdbers74315356
MSV3drs74315356
GWAS Ctlgrs74315356
Max Magnitude0
OMIM608309
Desc
Variant0002
Relatedalso
ClinVar
Risk rs74315356(A;A)
Alt rs74315356(A;A)
Reference rs74315356(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.20975547G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002507.2,