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rs16826658

From SNPedia

Orientationplus
Stabilizedplus
Make rs16826658(G;G)
Make rs16826658(G;T)
Make rs16826658(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position22159378
is asnp
is mentioned by
dbSNPrs16826658
ebirs16826658
HLIrs16826658
Exacrs16826658
Varsomers16826658
Maprs16826658
PheGenIrs16826658
hapmaprs16826658
1000 genomesrs16826658
hgdprs16826658
ensemblrs16826658
gopubmedrs16826658
geneviewrs16826658
scholarrs16826658
googlers16826658
pharmgkbrs16826658
gwascentralrs16826658
openSNPrs16826658
23andMers16826658
23andMe allrs16826658
SNP Nexus

SNPshotrs16826658
SNPdbers16826658
MSV3drs16826658
GWAS Ctlgrs16826658
GMAF0.3393
Max Magnitude
? (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