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rs17306692

From SNPedia

Orientationplus
Stabilizedplus
Make rs17306692(A;A)
Make rs17306692(A;C)
Make rs17306692(C;C)
ReferenceGRCh38 38.1/141
ChromosomeY
Position12018039
is asnp
is mentioned by
dbSNPrs17306692
dbSNP (classic)rs17306692
ClinGenrs17306692
ebirs17306692
HLIrs17306692
Exacrs17306692
Gnomadrs17306692
Varsomers17306692
LitVarrs17306692
Maprs17306692
PheGenIrs17306692
Biobankrs17306692
1000 genomesrs17306692
hgdprs17306692
ensemblrs17306692
geneviewrs17306692
scholarrs17306692
googlers17306692
pharmgkbrs17306692
gwascentralrs17306692
openSNPrs17306692
23andMers17306692
SNPshotrs17306692
SNPdbers17306692
MSV3drs17306692
GWAS Ctlgrs17306692
Y Chromrs17306692
GMAF0.02101
Max Magnitude0

[PMID 18385274] This snp distinguishes haplogroups


Haplogroup SNP
Alt. Name(s) L145, M449, PF6175
Source(s) None specified
Tree ISOGG build 12.211
Clade
Haplogroup
Haplogroup R (Y-DNA)
Ancestral
Haplogroup
Haplogroup R1 (Y-DNA)
Derived
Haplogroup
Haplogroup R1a (Y-DNA)
Ancestral Allele C
Derived Allele A