rs16980499
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | Relevant to haplogroup F-R |
Make rs16980499(C;C) |
Make rs16980499(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | Y |
Position | 15144138 |
is a | snp |
is | mentioned by |
dbSNP | rs16980499 |
dbSNP (classic) | rs16980499 |
ClinGen | rs16980499 |
ebi | rs16980499 |
HLI | rs16980499 |
Exac | rs16980499 |
Gnomad | rs16980499 |
Varsome | rs16980499 |
LitVar | rs16980499 |
Map | rs16980499 |
PheGenI | rs16980499 |
Biobank | rs16980499 |
1000 genomes | rs16980499 |
hgdp | rs16980499 |
ensembl | rs16980499 |
geneview | rs16980499 |
scholar | rs16980499 |
rs16980499 | |
pharmgkb | rs16980499 |
gwascentral | rs16980499 |
openSNP | rs16980499 |
23andMe | rs16980499 |
SNPshot | rs16980499 |
SNPdbe | rs16980499 |
MSV3d | rs16980499 |
GWAS Ctlg | rs16980499 |
Y Chrom | rs16980499 |
GMAF | 0.275 |
Max Magnitude | 0 |
[PMID 18385274] This snp distinguishes haplogroups