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rs295301

From SNPedia

Orientationplus
Stabilizedplus
Make rs295301(A;A)
Make rs295301(A;G)
Make rs295301(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position141619799
is asnp
is mentioned by
dbSNPrs295301
ebirs295301
HLIrs295301
Exacrs295301
Varsomers295301
Maprs295301
PheGenIrs295301
hapmaprs295301
1000 genomesrs295301
hgdprs295301
ensemblrs295301
gopubmedrs295301
geneviewrs295301
scholarrs295301
googlers295301
pharmgkbrs295301
gwascentralrs295301
openSNPrs295301
23andMers295301
23andMe allrs295301
SNP Nexus

SNPshotrs295301
SNPdbers295301
MSV3drs295301
GWAS Ctlgrs295301
GMAF0.3866
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 22210626OA-icon.png] Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP