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rs267606980

From SNPedia

Orientationplus
Stabilizedplus
Make rs267606980(G;G)
Make rs267606980(G;T)
Make rs267606980(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome20
Position4699600
GenePRNP
is asnp
is mentioned by
dbSNPrs267606980
dbSNP (old)rs267606980
ClinGenrs267606980
ebirs267606980
HLIrs267606980
Exacrs267606980
Varsomers267606980
Maprs267606980
PheGenIrs267606980
Biobankrs267606980
1000 genomesrs267606980
hgdprs267606980
ensemblrs267606980
gopubmedrs267606980
geneviewrs267606980
scholarrs267606980
googlers267606980
pharmgkbrs267606980
gwascentralrs267606980
openSNPrs267606980
23andMers267606980
23andMe allrs267606980
SNP Nexus

SNPshotrs267606980
SNPdbers267606980
MSV3drs267606980
GWAS Ctlgrs267606980
Max Magnitude
*rs267606980, G127V appears to protect against kuru [PMID 19923577]
ClinVar
Risk rs267606980(T;T)
Alt rs267606980(T;T)
Reference rs267606980(G;G)
Significance Other
Disease Kuru
Variation info
Gene PRNP
CLNDBN Kuru, protection against
Reversed 0
HGVS NC_000020.10:g.4680246G>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000014358.5,