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rs11799152

From SNPedia

Orientationplus
Stabilizedplus
Make rs11799152(A;A)
Make rs11799152(A;G)
Make rs11799152(G;G)
ReferenceGRCh38 38.1/141
ChromosomeY
Position12881443
is asnp
is mentioned by
dbSNPrs11799152
ebirs11799152
HLIrs11799152
Exacrs11799152
Varsomers11799152
Maprs11799152
PheGenIrs11799152
hapmaprs11799152
1000 genomesrs11799152
hgdprs11799152
ensemblrs11799152
gopubmedrs11799152
geneviewrs11799152
scholarrs11799152
googlers11799152
pharmgkbrs11799152
gwascentralrs11799152
openSNPrs11799152
23andMers11799152
23andMe allrs11799152
SNP Nexus

SNPshotrs11799152
SNPdbers11799152
MSV3drs11799152
GWAS Ctlgrs11799152
Y Chromrs11799152
GMAF0.01345
Max Magnitude

[PMID 19495413OA-icon.png] Improved resolution haplogroup G phylogeny in the Y chromosome, revealed by a set of newly characterized SNPs.