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rs121918297

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918297(C;T)
Make rs121918297(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position64223094
GeneFERMT3
is asnp
is mentioned by
dbSNPrs121918297
ebirs121918297
HLIrs121918297
Exacrs121918297
Varsomers121918297
Maprs121918297
PheGenIrs121918297
hapmaprs121918297
1000 genomesrs121918297
hgdprs121918297
ensemblrs121918297
gopubmedrs121918297
geneviewrs121918297
scholarrs121918297
googlers121918297
pharmgkbrs121918297
gwascentralrs121918297
openSNPrs121918297
23andMers121918297
23andMe allrs121918297
SNP Nexus

SNPshotrs121918297
SNPdbers121918297
MSV3drs121918297
GWAS Ctlgrs121918297
Max Magnitude0
OMIM607901
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121918297(T;T)
Alt rs121918297(T;T)
Reference rs121918297(C;C)
Significance Pathogenic
Disease Leukocyte adhesion deficiency
Variation info
Gene FERMT3
CLNDBN Leukocyte adhesion deficiency, type III
Reversed 0
HGVS NC_000011.9:g.63990566C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002829.2,