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rs121909338

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909338(C;T)
Make rs121909338(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position1610833
GeneFOXC1
is asnp
is mentioned by
dbSNPrs121909338
ebirs121909338
HLIrs121909338
Exacrs121909338
Varsomers121909338
Maprs121909338
PheGenIrs121909338
hapmaprs121909338
1000 genomesrs121909338
hgdprs121909338
ensemblrs121909338
gopubmedrs121909338
geneviewrs121909338
scholarrs121909338
googlers121909338
pharmgkbrs121909338
gwascentralrs121909338
openSNPrs121909338
23andMers121909338
23andMe allrs121909338
SNP Nexus

SNPshotrs121909338
SNPdbers121909338
MSV3drs121909338
GWAS Ctlgrs121909338
Max Magnitude0
OMIM601090
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121909338(T;T)
Alt rs121909338(T;T)
Reference rs121909338(C;C)
Significance Pathogenic
Disease Axenfeld-Rieger syndrome type 3 not provided
Variation info
Gene FOXC1
CLNDBN Axenfeld-Rieger syndrome type 3 not provided
Reversed 0
HGVS NC_000006.11:g.1611068C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008980.2, RCV000173256.1,