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rs2756271

From SNPedia

Orientationminus
Stabilizedminus
Make rs2756271(C;C)
Make rs2756271(C;T)
Make rs2756271(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position4684616
GenePRNP
is asnp
is mentioned by
dbSNPrs2756271
ebirs2756271
HLIrs2756271
Exacrs2756271
Varsomers2756271
Maprs2756271
PheGenIrs2756271
hapmaprs2756271
1000 genomesrs2756271
hgdprs2756271
ensemblrs2756271
gopubmedrs2756271
geneviewrs2756271
scholarrs2756271
googlers2756271
pharmgkbrs2756271
gwascentralrs2756271
openSNPrs2756271
23andMers2756271
23andMe allrs2756271
SNP Nexus

SNPshotrs2756271
SNPdbers2756271
MSV3drs2756271
GWAS Ctlgrs2756271
GMAF0.4123
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 22561193OA-icon.png] Genotype patterns and characteristics of PRNP in the Korean population


[PMID 18347820] Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutation.