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rs79691946

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs79691946(C;T)
Make rs79691946(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position1611334
GeneFOXC1
is asnp
is mentioned by
dbSNPrs79691946
ebirs79691946
HLIrs79691946
Exacrs79691946
Varsomers79691946
Maprs79691946
PheGenIrs79691946
hapmaprs79691946
1000 genomesrs79691946
hgdprs79691946
ensemblrs79691946
gopubmedrs79691946
geneviewrs79691946
scholarrs79691946
googlers79691946
pharmgkbrs79691946
gwascentralrs79691946
openSNPrs79691946
23andMers79691946
23andMe allrs79691946
SNP Nexus

SNPshotrs79691946
SNPdbers79691946
MSV3drs79691946
GWAS Ctlgrs79691946
GMAF0.03535
Max Magnitude0
ClinVar
Risk rs79691946(T;T)
Alt rs79691946(T;T)
Reference rs79691946(C;C)
Significance Pathogenic
Disease Iridogoniodysgenesis type1 not specified not provided
Variation info
Gene FOXC1
CLNDBN Iridogoniodysgenesis type1 not specified not provided
Reversed 0
HGVS NC_000006.11:g.1611569C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023070.2, RCV000153259.3, RCV000162086.1,