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rs886044143

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome6
Position1610735
GeneFOXC1
is asnp
is mentioned by
dbSNPrs886044143
dbSNP (classic)rs886044143
ClinGenrs886044143
ebirs886044143
HLIrs886044143
Exacrs886044143
Gnomadrs886044143
Varsomers886044143
LitVarrs886044143
Maprs886044143
PheGenIrs886044143
Biobankrs886044143
1000 genomesrs886044143
hgdprs886044143
ensemblrs886044143
geneviewrs886044143
scholarrs886044143
googlers886044143
pharmgkbrs886044143
gwascentralrs886044143
openSNPrs886044143
23andMers886044143
23andMe allrs886044143
SNPshotrs886044143
SNPdbers886044143
MSV3drs886044143
GWAS Ctlgrs886044143
Max Magnitude0
ClinVar
Risk rs886044143(A;A)
Alt rs886044143(A;A)
Reference Rs886044143(-;-)
Significance Pathogenic
Disease Axenfeld-Rieger syndrome type 3
Variation info
Gene FOXC1
CLNDBN Axenfeld-Rieger syndrome type 3
Reversed 0
HGVS NC_000006.11:g.1610970dupA
CLNSRC
CLNACC RCV000330894.1,