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rs74315352

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs74315352(A;C)
Make rs74315352(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position7984930
GenePARK7
is asnp
is mentioned by
dbSNPrs74315352
ebirs74315352
HLIrs74315352
Exacrs74315352
Varsomers74315352
Maprs74315352
PheGenIrs74315352
hapmaprs74315352
1000 genomesrs74315352
hgdprs74315352
ensemblrs74315352
gopubmedrs74315352
geneviewrs74315352
scholarrs74315352
googlers74315352
pharmgkbrs74315352
gwascentralrs74315352
openSNPrs74315352
23andMers74315352
23andMe allrs74315352
SNP Nexus

SNPshotrs74315352
SNPdbers74315352
MSV3drs74315352
GWAS Ctlgrs74315352
GMAF0.002296
Max Magnitude0
OMIM602533
Desc
Variant0004
Relatedalso
ClinVar
Risk rs74315352(C;C)
Alt rs74315352(C;C)
Reference rs74315352(A;A)
Significance Pathogenic
Disease Parkinson disease 7
Variation info
Gene PARK7
CLNDBN Parkinson disease 7
Reversed 0
HGVS NC_000001.10:g.8044990A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000007482.3,