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rs760676014

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs760676014(C;G)
Make rs760676014(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position1611936
GeneFOXC1
is asnp
is mentioned by
dbSNPrs760676014
dbSNP (classic)rs760676014
ClinGenrs760676014
ebirs760676014
HLIrs760676014
Exacrs760676014
Gnomadrs760676014
Varsomers760676014
LitVarrs760676014
Maprs760676014
PheGenIrs760676014
Biobankrs760676014
1000 genomesrs760676014
hgdprs760676014
ensemblrs760676014
geneviewrs760676014
scholarrs760676014
googlers760676014
pharmgkbrs760676014
gwascentralrs760676014
openSNPrs760676014
23andMers760676014
23andMe allrs760676014
SNPshotrs760676014
SNPdbers760676014
MSV3drs760676014
GWAS Ctlgrs760676014
Max Magnitude0
ClinVar
Risk rs760676014(G;G) rs760676014(T;T)
Alt rs760676014(G;G) rs760676014(T;T)
Reference Rs760676014(C;C)
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.1612171C>G
CLNSRC
CLNACC RCV000416548.1,