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rs121909336

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909336(A;A)
Make rs121909336(A;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position86510794
GeneFOXF1, FOXF1-AS1
is asnp
is mentioned by
dbSNPrs121909336
ebirs121909336
HLIrs121909336
Exacrs121909336
Varsomers121909336
Maprs121909336
PheGenIrs121909336
hapmaprs121909336
1000 genomesrs121909336
hgdprs121909336
ensemblrs121909336
gopubmedrs121909336
geneviewrs121909336
scholarrs121909336
googlers121909336
pharmgkbrs121909336
gwascentralrs121909336
openSNPrs121909336
23andMers121909336
23andMe allrs121909336
SNP Nexus

SNPshotrs121909336
SNPdbers121909336
MSV3drs121909336
GWAS Ctlgrs121909336
Max Magnitude0
OMIM601089
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909336(A;A)
Alt rs121909336(A;A)
Reference rs121909336(C;C)
Significance Pathogenic
Disease Alveolar capillary dysplasia with misalignment of pulmonary veins
Variation info
Gene FENDRR FOXF1
CLNDBN Alveolar capillary dysplasia with misalignment of pulmonary veins
Reversed 0
HGVS NC_000016.9:g.86544400C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008983.2,