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rs41469351

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41469351(C;T)
Make rs41469351(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position46370771
GeneCCR5, LOC102724297
is asnp
is mentioned by
dbSNPrs41469351
ebirs41469351
HLIrs41469351
Exacrs41469351
Varsomers41469351
Maprs41469351
PheGenIrs41469351
hapmaprs41469351
1000 genomesrs41469351
hgdprs41469351
ensemblrs41469351
gopubmedrs41469351
geneviewrs41469351
scholarrs41469351
googlers41469351
pharmgkbrs41469351
gwascentralrs41469351
openSNPrs41469351
23andMers41469351
23andMe allrs41469351
SNP Nexus

SNPshotrs41469351
SNPdbers41469351
MSV3drs41469351
GWAS Ctlgrs41469351
Max Magnitude0
ClinVar
Risk rs41469351(T;T)
Alt rs41469351(T;T)
Reference rs41469351(C;C)
Significance Pathogenic
Disease Human immunodeficiency virus type 1
Variation info
Gene LOC102724297 CCR5
CLNDBN Human immunodeficiency virus type 1, increased perinatal transmission of
Reversed 0
HGVS NC_000003.11:g.46412262C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008672.2,