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rs387906400

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906400(A;A)
Make rs387906400(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position44378102
GeneCXCL12
is asnp
is mentioned by
dbSNPrs387906400
ebirs387906400
HLIrs387906400
Exacrs387906400
Varsomers387906400
Maprs387906400
PheGenIrs387906400
hapmaprs387906400
1000 genomesrs387906400
hgdprs387906400
ensemblrs387906400
gopubmedrs387906400
geneviewrs387906400
scholarrs387906400
googlers387906400
pharmgkbrs387906400
gwascentralrs387906400
openSNPrs387906400
23andMers387906400
23andMe allrs387906400
SNP Nexus

SNPshotrs387906400
SNPdbers387906400
MSV3drs387906400
GWAS Ctlgrs387906400
Max Magnitude0
ClinVar
Risk rs387906400(A;A)
Alt rs387906400(A;A)
Reference rs387906400(G;G)
Significance Other
Disease Human immunodeficiency virus type 1
Variation info
Gene CXCL12
CLNDBN Human immunodeficiency virus type 1, susceptibility to
Reversed 1
HGVS NC_000010.10:g.44873550C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009307.3,