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rs74315360

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs74315360(A;A)
Make rs74315360(A;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position20638104
GenePINK1
is asnp
is mentioned by
dbSNPrs74315360
ebirs74315360
HLIrs74315360
Exacrs74315360
Varsomers74315360
Maprs74315360
PheGenIrs74315360
hapmaprs74315360
1000 genomesrs74315360
hgdprs74315360
ensemblrs74315360
gopubmedrs74315360
geneviewrs74315360
scholarrs74315360
googlers74315360
pharmgkbrs74315360
gwascentralrs74315360
openSNPrs74315360
23andMers74315360
23andMe allrs74315360
SNP Nexus

SNPshotrs74315360
SNPdbers74315360
MSV3drs74315360
GWAS Ctlgrs74315360
Max Magnitude0
OMIM608309
Desc
Variant0011
Relatedalso
ClinVar
Risk rs74315360(A;A)
Alt rs74315360(A;A)
Reference rs74315360(C;C)
Significance Pathogenic
Disease Parkinson disease 6
Variation info
Gene PINK1
CLNDBN Parkinson disease 6, autosomal recessive early-onset
Reversed 0
HGVS NC_000001.10:g.20964597C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002515.3,