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rs886039568

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs886039568(C;T)
Make rs886039568(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome6
Position1610701
GeneFOXC1
is asnp
is mentioned by
dbSNPrs886039568
dbSNP (classic)rs886039568
ClinGenrs886039568
ebirs886039568
HLIrs886039568
Exacrs886039568
Gnomadrs886039568
Varsomers886039568
LitVarrs886039568
Maprs886039568
PheGenIrs886039568
Biobankrs886039568
1000 genomesrs886039568
hgdprs886039568
ensemblrs886039568
geneviewrs886039568
scholarrs886039568
googlers886039568
pharmgkbrs886039568
gwascentralrs886039568
openSNPrs886039568
23andMers886039568
23andMe allrs886039568
SNPshotrs886039568
SNPdbers886039568
MSV3drs886039568
GWAS Ctlgrs886039568
Max Magnitude0
ClinVar
Risk rs886039568(T;T)
Alt rs886039568(T;T)
Reference Rs886039568(C;C)
Significance Pathogenic
Disease not provided Axenfeld-Rieger syndrome type 3
Variation info
Gene FOXC1
CLNDBN not provided Axenfeld-Rieger syndrome type 3
Reversed 0
HGVS NC_000006.11:g.1610936C>T
CLNSRC
CLNACC RCV000255576.1, RCV000416497.1,