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rs6776297

From SNPedia

Orientationplus
Stabilizedplus
Make rs6776297(A;A)
Make rs6776297(A;G)
Make rs6776297(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position32336779
GeneCMTM8
is asnp
is mentioned by
dbSNPrs6776297
dbSNP (classic)rs6776297
ClinGenrs6776297
ebirs6776297
HLIrs6776297
Exacrs6776297
Gnomadrs6776297
Varsomers6776297
LitVarrs6776297
Maprs6776297
PheGenIrs6776297
Biobankrs6776297
1000 genomesrs6776297
hgdprs6776297
ensemblrs6776297
geneviewrs6776297
scholarrs6776297
googlers6776297
pharmgkbrs6776297
gwascentralrs6776297
openSNPrs6776297
23andMers6776297
SNPshotrs6776297
SNPdbers6776297
MSV3drs6776297
GWAS Ctlgrs6776297
GMAF0.2319
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 22174851OA-icon.png]
Trait
Title Genomewide association study for determinants of HIV-1 acquisition and viral set point in HIV-1 serodiscordant couples with quantified virus exposure.
Risk Allele
P-val 0.000005
Odds Ratio None None