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rs7758512

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs7758512(G;G)
Make rs7758512(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position30002812
GeneZNRD1-AS1
is asnp
is mentioned by
dbSNPrs7758512
ebirs7758512
HLIrs7758512
Exacrs7758512
Varsomers7758512
Maprs7758512
PheGenIrs7758512
hapmaprs7758512
1000 genomesrs7758512
hgdprs7758512
ensemblrs7758512
gopubmedrs7758512
geneviewrs7758512
scholarrs7758512
googlers7758512
pharmgkbrs7758512
gwascentralrs7758512
openSNPrs7758512
23andMers7758512
23andMe allrs7758512
SNP Nexus

SNPshotrs7758512
SNPdbers7758512
MSV3drs7758512
GWAS Ctlgrs7758512
GMAF0.1846
Max Magnitude0
? (G;G) (G;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 2E-8
Odds Ratio NR NR


[PMID 18495769OA-icon.png] Transmission of human immunodeficiency virus type 1 from a patient who developed AIDS to an elite suppressor.


[PMID 19197363OA-icon.png] A genome-wide investigation of SNPs and CNVs in schizophrenia.


GET Evidence
rs7758512
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.195312
summary