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rs121918296

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918296(A;A)
Make rs121918296(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position64207412
GeneFERMT3
is asnp
is mentioned by
dbSNPrs121918296
ebirs121918296
HLIrs121918296
Exacrs121918296
Varsomers121918296
Maprs121918296
PheGenIrs121918296
hapmaprs121918296
1000 genomesrs121918296
hgdprs121918296
ensemblrs121918296
gopubmedrs121918296
geneviewrs121918296
scholarrs121918296
googlers121918296
pharmgkbrs121918296
gwascentralrs121918296
openSNPrs121918296
23andMers121918296
23andMe allrs121918296
SNP Nexus

SNPshotrs121918296
SNPdbers121918296
MSV3drs121918296
GWAS Ctlgrs121918296
Max Magnitude0
OMIM607901
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121918296(A;A)
Alt rs121918296(A;A)
Reference rs121918296(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.63974884G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002828.2,