Have questions? Visit https://www.reddit.com/r/SNPedia

rs4932217

From SNPedia

Orientationplus
Stabilizedplus
Make rs4932217(A;A)
Make rs4932217(A;C)
Make rs4932217(C;C)
ReferenceGRCh38 38.1/141
Chromosome15
Position89358801
GeneLOC100288864
is asnp
is mentioned by
dbSNPrs4932217
ebirs4932217
HLIrs4932217
Exacrs4932217
Varsomers4932217
Maprs4932217
PheGenIrs4932217
hapmaprs4932217
1000 genomesrs4932217
hgdprs4932217
ensemblrs4932217
gopubmedrs4932217
geneviewrs4932217
scholarrs4932217
googlers4932217
pharmgkbrs4932217
gwascentralrs4932217
openSNPrs4932217
23andMers4932217
23andMe allrs4932217
SNP Nexus

SNPshotrs4932217
SNPdbers4932217
MSV3drs4932217
GWAS Ctlgrs4932217
GMAF0.4931
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS
SNP rs4932217
PubMedID [PMID 18193045OA-icon.png]
Condition Height
Gene POLG
Risk Allele A
pValue 8.00E-007
OR 0.66
95% CI NR) cm talle



GET Evidence
rs4932217
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.62931
summary