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rs5990560

From SNPedia

Orientationplus
Stabilizedplus
Make rs5990560(A;A)
Make rs5990560(A;T)
Make rs5990560(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position96406563
is asnp
is mentioned by
dbSNPrs5990560
ebirs5990560
HLIrs5990560
Exacrs5990560
Varsomers5990560
Maprs5990560
PheGenIrs5990560
hapmaprs5990560
1000 genomesrs5990560
hgdprs5990560
ensemblrs5990560
gopubmedrs5990560
geneviewrs5990560
scholarrs5990560
googlers5990560
pharmgkbrs5990560
gwascentralrs5990560
openSNPrs5990560
23andMers5990560
23andMe allrs5990560
SNP Nexus

SNPshotrs5990560
SNPdbers5990560
MSV3drs5990560
GWAS Ctlgrs5990560
GMAF0.3567
Max Magnitude
? (A;A) (A;T) (T;T) 28

[PMID 22177906] Development of multiplex assay with 16 SNPs on X chromosome for degraded samples