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rs55830907

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs55830907(C;T)
Make rs55830907(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position161360169
GenePARK2
is asnp
is mentioned by
dbSNPrs55830907
dbSNP (classic)rs55830907
ClinGenrs55830907
ebirs55830907
HLIrs55830907
Exacrs55830907
Gnomadrs55830907
Varsomers55830907
LitVarrs55830907
Maprs55830907
PheGenIrs55830907
Biobankrs55830907
1000 genomesrs55830907
hgdprs55830907
ensemblrs55830907
geneviewrs55830907
scholarrs55830907
googlers55830907
pharmgkbrs55830907
gwascentralrs55830907
openSNPrs55830907
23andMers55830907
SNPshotrs55830907
SNPdbers55830907
MSV3drs55830907
GWAS Ctlgrs55830907
Max Magnitude0
ClinVar
Risk rs55830907(T;T)
Alt rs55830907(T;T)
Reference Rs55830907(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PARK2
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.161781201G>A
CLNSRC
CLNACC RCV000487928.1,