rs16826658
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs16826658(G;G) |
Make rs16826658(G;T) |
Make rs16826658(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 22159378 |
Gene | LOC105376850 |
is a | snp |
is | mentioned by |
dbSNP | rs16826658 |
dbSNP (classic) | rs16826658 |
ClinGen | rs16826658 |
ebi | rs16826658 |
HLI | rs16826658 |
Exac | rs16826658 |
Gnomad | rs16826658 |
Varsome | rs16826658 |
LitVar | rs16826658 |
Map | rs16826658 |
PheGenI | rs16826658 |
Biobank | rs16826658 |
1000 genomes | rs16826658 |
hgdp | rs16826658 |
ensembl | rs16826658 |
geneview | rs16826658 |
scholar | rs16826658 |
rs16826658 | |
pharmgkb | rs16826658 |
gwascentral | rs16826658 |
openSNP | rs16826658 |
23andMe | rs16826658 |
SNPshot | rs16826658 |
SNPdbe | rs16826658 |
MSV3d | rs16826658 |
GWAS Ctlg | rs16826658 |
GMAF | 0.3393 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 20601957] A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese
[PMID 25682310] Analysis of WNT4 polymorphism in Chinese Han women with endometriosis