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rs55777503

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs55777503(-;-)
Make rs55777503(-;AG)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position162443379
GenePARK2
is asnp
is mentioned by
dbSNPrs55777503
dbSNP (classic)rs55777503
ClinGenrs55777503
ebirs55777503
HLIrs55777503
Exacrs55777503
Gnomadrs55777503
Varsomers55777503
LitVarrs55777503
Maprs55777503
PheGenIrs55777503
Biobankrs55777503
1000 genomesrs55777503
hgdprs55777503
ensemblrs55777503
geneviewrs55777503
scholarrs55777503
googlers55777503
pharmgkbrs55777503
gwascentralrs55777503
openSNPrs55777503
23andMers55777503
SNPshotrs55777503
SNPdbers55777503
MSV3drs55777503
GWAS Ctlgrs55777503
Max Magnitude0
ClinVar
Risk rs55777503(-;-)
Alt rs55777503(-;-)
Reference Rs55777503(AG;AG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PARK2
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.162864411_162864412delCT
CLNSRC
CLNACC RCV000488202.1,