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rs104893625

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893625(G;T)
Make rs104893625(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position136114901
GeneCXCR4
is asnp
is mentioned by
dbSNPrs104893625
ebirs104893625
HLIrs104893625
Exacrs104893625
Varsomers104893625
Maprs104893625
PheGenIrs104893625
hapmaprs104893625
1000 genomesrs104893625
hgdprs104893625
ensemblrs104893625
gopubmedrs104893625
geneviewrs104893625
scholarrs104893625
googlers104893625
pharmgkbrs104893625
gwascentralrs104893625
openSNPrs104893625
23andMers104893625
23andMe allrs104893625
SNP Nexus

SNPshotrs104893625
SNPdbers104893625
MSV3drs104893625
GWAS Ctlgrs104893625
Max Magnitude0
OMIM162643
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104893625(T;T)
Alt rs104893625(T;T)
Reference rs104893625(G;G)
Significance Pathogenic
Disease Warts
Variation info
Gene CXCR4
CLNDBN Warts, hypogammaglobulinemia, infections, and myelokathexis
Reversed 1
HGVS NC_000002.11:g.136872471C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015066.26,