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rs1044165

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0
Make rs1044165(C;T)
Make rs1044165(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position66021884
GeneVSIG4
is asnp
is mentioned by
dbSNPrs1044165
ebirs1044165
HLIrs1044165
Exacrs1044165
Varsomers1044165
Maprs1044165
PheGenIrs1044165
hapmaprs1044165
1000 genomesrs1044165
hgdprs1044165
ensemblrs1044165
gopubmedrs1044165
geneviewrs1044165
scholarrs1044165
googlers1044165
pharmgkbrs1044165
gwascentralrs1044165
openSNPrs1044165
23andMers1044165
23andMe allrs1044165
SNP Nexus

SNPshotrs1044165
SNPdbers1044165
MSV3drs1044165
GWAS Ctlgrs1044165
GMAF0.06711
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 23439547OA-icon.png] Expression and Genetic Analysis of MicroRNAs Involved in Multiple Sclerosis


[PMID 15902657OA-icon.png] Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia.


[PMID 26305248OA-icon.png] Variants of MicroRNA Genes: Gender-Specific Associations with Multiple Sclerosis Risk and Severity