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rs137852610

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852610(A;C)
Make rs137852610(C;C)
ReferenceGRCh38 38.1/141
Chromosome21
Position44901646
GeneITGB2
is asnp
is mentioned by
dbSNPrs137852610
ebirs137852610
HLIrs137852610
Exacrs137852610
Varsomers137852610
Maprs137852610
PheGenIrs137852610
hapmaprs137852610
1000 genomesrs137852610
hgdprs137852610
ensemblrs137852610
gopubmedrs137852610
geneviewrs137852610
scholarrs137852610
googlers137852610
pharmgkbrs137852610
gwascentralrs137852610
openSNPrs137852610
23andMers137852610
23andMe allrs137852610
SNP Nexus

SNPshotrs137852610
SNPdbers137852610
MSV3drs137852610
GWAS Ctlgrs137852610
Max Magnitude0
OMIM600065
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137852610(C;C)
Alt rs137852610(C;C)
Reference rs137852610(A;A)
Significance Pathogenic
Disease Leukocyte adhesion deficiency
Variation info
Gene ITGB2
CLNDBN Leukocyte adhesion deficiency
Reversed 1
HGVS NC_000021.8:g.46321561T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010067.2,