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rs104893626

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893626(C;G)
Make rs104893626(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position136114915
GeneCXCR4
is asnp
is mentioned by
dbSNPrs104893626
ebirs104893626
HLIrs104893626
Exacrs104893626
Varsomers104893626
Maprs104893626
PheGenIrs104893626
hapmaprs104893626
1000 genomesrs104893626
hgdprs104893626
ensemblrs104893626
gopubmedrs104893626
geneviewrs104893626
scholarrs104893626
googlers104893626
pharmgkbrs104893626
gwascentralrs104893626
openSNPrs104893626
23andMers104893626
23andMe allrs104893626
SNP Nexus

SNPshotrs104893626
SNPdbers104893626
MSV3drs104893626
GWAS Ctlgrs104893626
Max Magnitude0
OMIM162643
Desc
Variant0004
Relatedalso
ClinVar
Risk rs104893626(G;G)
Alt rs104893626(G;G)
Reference rs104893626(C;C)
Significance Pathogenic
Disease Warts
Variation info
Gene CXCR4
CLNDBN Warts, hypogammaglobulinemia, infections, and myelokathexis
Reversed 1
HGVS NC_000002.11:g.136872485G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000015067.26,