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

rs1800560

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1800560(A;A)
Make rs1800560(A;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position46373205
GeneCCR5, LOC102724297
is asnp
is mentioned by
dbSNPrs1800560
ebirs1800560
HLIrs1800560
Exacrs1800560
Varsomers1800560
Maprs1800560
PheGenIrs1800560
hapmaprs1800560
1000 genomesrs1800560
hgdprs1800560
ensemblrs1800560
gopubmedrs1800560
geneviewrs1800560
scholarrs1800560
googlers1800560
pharmgkbrs1800560
gwascentralrs1800560
openSNPrs1800560
23andMers1800560
23andMe allrs1800560
SNP Nexus

SNPshotrs1800560
SNPdbers1800560
MSV3drs1800560
GWAS Ctlgrs1800560
GMAF0.0
Max Magnitude0
OMIM601373
Desc
Variant0005
Relatedalso
ClinVar
Risk rs1800560(A;A)
Alt rs1800560(A;A)
Reference rs1800560(T;T)
Significance Other
Disease Human immunodeficiency virus type 1
Variation info
Gene LOC102724297 CCR5
CLNDBN Human immunodeficiency virus type 1, susceptibility to
Reversed 0
HGVS NC_000003.11:g.46414696T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008670.3,