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rs4116821

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) Relevant to haplogroup P
Make rs4116821(C;C)
Make rs4116821(C;G)
ReferenceGRCh38 38.1/141
ChromosomeY
Position19910454
is asnp
is mentioned by
dbSNPrs4116821
dbSNP (classic)rs4116821
ClinGenrs4116821
ebirs4116821
HLIrs4116821
Exacrs4116821
Gnomadrs4116821
Varsomers4116821
LitVarrs4116821
Maprs4116821
PheGenIrs4116821
Biobankrs4116821
1000 genomesrs4116821
hgdprs4116821
ensemblrs4116821
geneviewrs4116821
scholarrs4116821
googlers4116821
pharmgkbrs4116821
gwascentralrs4116821
openSNPrs4116821
23andMers4116821
SNPshotrs4116821
SNPdbers4116821
MSV3drs4116821
GWAS Ctlgrs4116821
Y Chromrs4116821
GMAF0.2634
Max Magnitude0
? (C;C) (C;G) (G;G) 28


[PMID 18385274] This snp distinguishes haplogroups



Haplogroup SNP
Alt. Name(s) P284
Source(s) None specified
Tree ISOGG build 5
Clade
Haplogroup
Haplogroup P (Y-DNA)
Ancestral
Haplogroup
Haplogroup NOP (Y-DNA)
Derived
Haplogroup
Haplogroup P (Y-DNA)
Ancestral Allele C
Derived Allele G



[PMID 18076761OA-icon.png] In silico and in vitro comparative analysis to select, validate and test SNPs for human identification.