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rs137852616

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852616(A;A)
Make rs137852616(A;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position44900367
GeneITGB2
is asnp
is mentioned by
dbSNPrs137852616
ebirs137852616
HLIrs137852616
Exacrs137852616
Varsomers137852616
Maprs137852616
PheGenIrs137852616
hapmaprs137852616
1000 genomesrs137852616
hgdprs137852616
ensemblrs137852616
gopubmedrs137852616
geneviewrs137852616
scholarrs137852616
googlers137852616
pharmgkbrs137852616
gwascentralrs137852616
openSNPrs137852616
23andMers137852616
23andMe allrs137852616
SNP Nexus

SNPshotrs137852616
SNPdbers137852616
MSV3drs137852616
GWAS Ctlgrs137852616
Max Magnitude0
OMIM600065
Desc
Variant0012
Relatedalso
ClinVar
Risk rs137852616(A;A)
Alt rs137852616(A;A)
Reference rs137852616(G;G)
Significance Pathogenic
Disease Leukocyte adhesion deficiency
Variation info
Gene ITGB2
CLNDBN Leukocyte adhesion deficiency
Reversed 1
HGVS NC_000021.8:g.46320282C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010077.2,