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rs121918298

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918298(A;A)
Make rs121918298(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position64211648
GeneFERMT3
is asnp
is mentioned by
dbSNPrs121918298
ebirs121918298
HLIrs121918298
Exacrs121918298
Varsomers121918298
Maprs121918298
PheGenIrs121918298
hapmaprs121918298
1000 genomesrs121918298
hgdprs121918298
ensemblrs121918298
gopubmedrs121918298
geneviewrs121918298
scholarrs121918298
googlers121918298
pharmgkbrs121918298
gwascentralrs121918298
openSNPrs121918298
23andMers121918298
23andMe allrs121918298
SNP Nexus

SNPshotrs121918298
SNPdbers121918298
MSV3drs121918298
GWAS Ctlgrs121918298
Max Magnitude0
OMIM607901
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121918298(A;A)
Alt rs121918298(A;A)
Reference rs121918298(G;G)
Significance Pathogenic
Disease Leukocyte adhesion deficiency
Variation info
Gene FERMT3
CLNDBN Leukocyte adhesion deficiency, type III
Reversed 0
HGVS NC_000011.9:g.63979120G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002830.2,