rs9785913
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | Relevant to haplogroup F-R |
Make rs9785913(C;C) |
Make rs9785913(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | Y |
Position | 15381633 |
Gene | LOC100287953 |
is a | snp |
is | mentioned by |
dbSNP | rs9785913 |
dbSNP (classic) | rs9785913 |
ClinGen | rs9785913 |
ebi | rs9785913 |
HLI | rs9785913 |
Exac | rs9785913 |
Gnomad | rs9785913 |
Varsome | rs9785913 |
LitVar | rs9785913 |
Map | rs9785913 |
PheGenI | rs9785913 |
Biobank | rs9785913 |
1000 genomes | rs9785913 |
hgdp | rs9785913 |
ensembl | rs9785913 |
geneview | rs9785913 |
scholar | rs9785913 |
rs9785913 | |
pharmgkb | rs9785913 |
gwascentral | rs9785913 |
openSNP | rs9785913 |
23andMe | rs9785913 |
SNPshot | rs9785913 |
SNPdbe | rs9785913 |
MSV3d | rs9785913 |
GWAS Ctlg | rs9785913 |
Y Chrom | rs9785913 |
GMAF | 0.2646 |
Max Magnitude | 0 |
[PMID 18385274] This snp distinguishes haplogroups