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rs16948255

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs16948255(C;T)
Make rs16948255(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position74847922
is asnp
is mentioned by
dbSNPrs16948255
dbSNP (classic)rs16948255
ClinGenrs16948255
ebirs16948255
HLIrs16948255
Exacrs16948255
Gnomadrs16948255
Varsomers16948255
LitVarrs16948255
Maprs16948255
PheGenIrs16948255
Biobankrs16948255
1000 genomesrs16948255
hgdprs16948255
ensemblrs16948255
geneviewrs16948255
scholarrs16948255
googlers16948255
pharmgkbrs16948255
gwascentralrs16948255
openSNPrs16948255
23andMers16948255
SNPshotrs16948255
SNPdbers16948255
MSV3drs16948255
GWAS Ctlgrs16948255
GMAF0.02847
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 20041166OA-icon.png]
Trait HIV-1 control
Title Common Genetic Variation and the Control of HIV-1 in Human
Risk Allele
P-val 0.000001
Odds Ratio NR NR