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rs373653682

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GTGCTGGACGGTGTCCCT;GTGCTGGACGGTGTCCCT) 0 common in clinvar
(TGTGCTGGACGGTGTCCC;TGTGCTGGACGGTGTCCC) 0 common in clinvar
Make rs373653682(-;-)
Make rs373653682(-;TGTGCTGGACGGTGTCCC)
ReferenceGRCh38 38.1/141
Chromosome1
Position7961868
GenePARK7
is asnp
is mentioned by
dbSNPrs373653682
dbSNP (old)rs373653682
ClinGenrs373653682
ebirs373653682
HLIrs373653682
Exacrs373653682
Varsomers373653682
Maprs373653682
PheGenIrs373653682
Biobankrs373653682
1000 genomesrs373653682
hgdprs373653682
ensemblrs373653682
gopubmedrs373653682
geneviewrs373653682
scholarrs373653682
googlers373653682
pharmgkbrs373653682
gwascentralrs373653682
openSNPrs373653682
23andMers373653682
23andMe allrs373653682
SNP Nexus

SNPshotrs373653682
SNPdbers373653682
MSV3drs373653682
GWAS Ctlgrs373653682
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs373653682(GTGCTGGACGGTGTCCCT;GTGCTGGACGGTGTCCCT)
Significance Pathogenic
Disease Parkinson disease 7
Variation info
Gene PARK7
CLNDBN Parkinson disease 7
Reversed 0
HGVS NC_000001.11:g.7961868_7961885dup18
CLNSRC ClinVar
CLNACC RCV000007484.1,