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rs74315357

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs74315357(C;T)
Make rs74315357(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position20639952
GenePINK1
is asnp
is mentioned by
dbSNPrs74315357
ebirs74315357
HLIrs74315357
Exacrs74315357
Varsomers74315357
Maprs74315357
PheGenIrs74315357
hapmaprs74315357
1000 genomesrs74315357
hgdprs74315357
ensemblrs74315357
gopubmedrs74315357
geneviewrs74315357
scholarrs74315357
googlers74315357
pharmgkbrs74315357
gwascentralrs74315357
openSNPrs74315357
23andMers74315357
23andMe allrs74315357
SNP Nexus

SNPshotrs74315357
SNPdbers74315357
MSV3drs74315357
GWAS Ctlgrs74315357
Max Magnitude0
OMIM608309
Desc
Variant0003
Relatedalso
ClinVar
Risk rs74315357(A,T;A,T)
Alt rs74315357(A,T;A,T)
Reference rs74315357(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.20966445C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002508.3,