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rs3862227

From SNPedia

Orientationplus
Stabilizedplus
Make rs3862227(A;A)
Make rs3862227(A;G)
Make rs3862227(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position43255323
GeneTMLHE
is asnp
is mentioned by
dbSNPrs3862227
ebirs3862227
HLIrs3862227
Exacrs3862227
Varsomers3862227
Maprs3862227
PheGenIrs3862227
hapmaprs3862227
1000 genomesrs3862227
hgdprs3862227
ensemblrs3862227
gopubmedrs3862227
geneviewrs3862227
scholarrs3862227
googlers3862227
pharmgkbrs3862227
gwascentralrs3862227
openSNPrs3862227
23andMers3862227
23andMe allrs3862227
SNP Nexus

SNPshotrs3862227
SNPdbers3862227
MSV3drs3862227
GWAS Ctlgrs3862227
GMAF0.3604
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 15986317OA-icon.png] Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease.


GET Evidence
rs3862227
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.28125
summary