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rs4709583

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs4709583(A;G)
Make rs4709583(G;G)
ReferenceGRCh38 38.1/142
Chromosome6
Position162201272
GenePARK2
is asnp
is mentioned by
dbSNPrs4709583
dbSNP (old)rs4709583
ClinGenrs4709583
ebirs4709583
HLIrs4709583
Exacrs4709583
Gnomadrs4709583
Varsomers4709583
Maprs4709583
PheGenIrs4709583
Biobankrs4709583
1000 genomesrs4709583
hgdprs4709583
ensemblrs4709583
gopubmedrs4709583
geneviewrs4709583
scholarrs4709583
googlers4709583
pharmgkbrs4709583
gwascentralrs4709583
openSNPrs4709583
23andMers4709583
23andMe allrs4709583
SNP Nexus

SNPshotrs4709583
SNPdbers4709583
MSV3drs4709583
GWAS Ctlgrs4709583
Max Magnitude0

[PMID 24861865] Genetic variants in apoptosis-related genes associated with colorectal hyperplasia


ClinVar
Risk rs4709583(G;G)
Alt rs4709583(G;G)
Reference Rs4709583(A;A)
Significance Non-pathogenic
Disease not specified
Variation info
Gene PARK2
CLNDBN not specified
Reversed 0
HGVS NC_000006.11:g.162622304A>G
CLNSRC
CLNACC RCV000249119.1,