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rs2071598

From SNPedia

Orientationminus
Stabilizedminus
Make rs2071598(A;A)
Make rs2071598(A;C)
Make rs2071598(C;C)
ReferenceGRCh38 38.1/141
Chromosome8
Position98117279
GeneHRSP12, POP1
is asnp
is mentioned by
dbSNPrs2071598
ebirs2071598
HLIrs2071598
Exacrs2071598
Varsomers2071598
Maprs2071598
PheGenIrs2071598
hapmaprs2071598
1000 genomesrs2071598
hgdprs2071598
ensemblrs2071598
gopubmedrs2071598
geneviewrs2071598
scholarrs2071598
googlers2071598
pharmgkbrs2071598
gwascentralrs2071598
openSNPrs2071598
23andMers2071598
23andMe allrs2071598
SNP Nexus

SNPshotrs2071598
SNPdbers2071598
MSV3drs2071598
GWAS Ctlgrs2071598
GMAF0.1869
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 22210626OA-icon.png]
Trait
Title Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.
Risk Allele
P-val 0.000009
Odds Ratio 1.2646 None