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rs121909107

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909107(A;A)
Make rs121909107(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position86567697
GeneFOXC2
is asnp
is mentioned by
dbSNPrs121909107
ebirs121909107
HLIrs121909107
Exacrs121909107
Varsomers121909107
Maprs121909107
PheGenIrs121909107
hapmaprs121909107
1000 genomesrs121909107
hgdprs121909107
ensemblrs121909107
gopubmedrs121909107
geneviewrs121909107
scholarrs121909107
googlers121909107
pharmgkbrs121909107
gwascentralrs121909107
openSNPrs121909107
23andMers121909107
23andMe allrs121909107
SNP Nexus

SNPshotrs121909107
SNPdbers121909107
MSV3drs121909107
GWAS Ctlgrs121909107
Max Magnitude0
OMIM602402
Desc
Variant0013
Relatedalso
ClinVar
Risk rs121909107(A;A)
Alt rs121909107(A;A)
Reference rs121909107(G;G)
Significance Pathogenic
Disease Distichiasis-lymphedema syndrome
Variation info
Gene FOXC2 FOXC2-AS1
CLNDBN Distichiasis-lymphedema syndrome
Reversed 0
HGVS NC_000016.9:g.86601303G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007683.2,