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rs1800940

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1800940(G;T)
Make rs1800940(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position46373082
GeneCCR5, LOC102724297
is asnp
is mentioned by
dbSNPrs1800940
ebirs1800940
HLIrs1800940
Exacrs1800940
Varsomers1800940
Maprs1800940
PheGenIrs1800940
hapmaprs1800940
1000 genomesrs1800940
hgdprs1800940
ensemblrs1800940
gopubmedrs1800940
geneviewrs1800940
scholarrs1800940
googlers1800940
pharmgkbrs1800940
gwascentralrs1800940
openSNPrs1800940
23andMers1800940
23andMe allrs1800940
SNP Nexus

SNPshotrs1800940
SNPdbers1800940
MSV3drs1800940
GWAS Ctlgrs1800940
Max Magnitude0
OMIM601373
Desc
Variant0008
Relatedalso
ClinVar
Risk rs1800940(T;T)
Alt rs1800940(T;T)
Reference rs1800940(G;G)
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.46414573G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008673.4,