Have questions? Visit https://www.reddit.com/r/SNPedia

rs4827155

From SNPedia

Orientationplus
Stabilizedplus
Make rs4827155(C;C)
Make rs4827155(C;T)
Make rs4827155(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position39449692
is asnp
is mentioned by
dbSNPrs4827155
ebirs4827155
HLIrs4827155
Exacrs4827155
Varsomers4827155
Maprs4827155
PheGenIrs4827155
hapmaprs4827155
1000 genomesrs4827155
hgdprs4827155
ensemblrs4827155
gopubmedrs4827155
geneviewrs4827155
scholarrs4827155
googlers4827155
pharmgkbrs4827155
gwascentralrs4827155
openSNPrs4827155
23andMers4827155
23andMe allrs4827155
SNP Nexus

SNPshotrs4827155
SNPdbers4827155
MSV3drs4827155
GWAS Ctlgrs4827155
GMAF0.4855
Max Magnitude
? (C;C) (C;T) (T;T) 28

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