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rs121909337

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909337(C;C)
Make rs121909337(C;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position86513083
GeneFOXF1
is asnp
is mentioned by
dbSNPrs121909337
ebirs121909337
HLIrs121909337
Exacrs121909337
Varsomers121909337
Maprs121909337
PheGenIrs121909337
hapmaprs121909337
1000 genomesrs121909337
hgdprs121909337
ensemblrs121909337
gopubmedrs121909337
geneviewrs121909337
scholarrs121909337
googlers121909337
pharmgkbrs121909337
gwascentralrs121909337
openSNPrs121909337
23andMers121909337
23andMe allrs121909337
SNP Nexus

SNPshotrs121909337
SNPdbers121909337
MSV3drs121909337
GWAS Ctlgrs121909337
Max Magnitude0
OMIM601089
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121909337(C;C)
Alt rs121909337(C;C)
Reference rs121909337(T;T)
Significance Pathogenic
Disease Alveolar capillary dysplasia with misalignment of pulmonary veins
Variation info
Gene FOXF1
CLNDBN Alveolar capillary dysplasia with misalignment of pulmonary veins
Reversed 0
HGVS NC_000016.9:g.86546689T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000008984.3,