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rs2987763

From SNPedia

Orientationplus
Stabilizedplus
Make rs2987763(A;A)
Make rs2987763(A;T)
Make rs2987763(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position153313558
is asnp
is mentioned by
dbSNPrs2987763
ebirs2987763
HLIrs2987763
Exacrs2987763
Varsomers2987763
Maprs2987763
PheGenIrs2987763
hapmaprs2987763
1000 genomesrs2987763
hgdprs2987763
ensemblrs2987763
gopubmedrs2987763
geneviewrs2987763
scholarrs2987763
googlers2987763
pharmgkbrs2987763
gwascentralrs2987763
openSNPrs2987763
23andMers2987763
23andMe allrs2987763
SNP Nexus

SNPshotrs2987763
SNPdbers2987763
MSV3drs2987763
GWAS Ctlgrs2987763
Max Magnitude
? (A;A) (A;T) (T;T) 28

[PMID 24838182] Peptidoglycan recognition protein genes and risk of Parkinson's disease