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rs1057518738

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518738(A;A)
Make rs1057518738(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position47416622
GeneFOXE3, LINC01389
is asnp
is mentioned by
dbSNPrs1057518738
dbSNP (old)rs1057518738
ClinGenrs1057518738
ebirs1057518738
HLIrs1057518738
Exacrs1057518738
Gnomadrs1057518738
Varsomers1057518738
Maprs1057518738
PheGenIrs1057518738
Biobankrs1057518738
1000 genomesrs1057518738
hgdprs1057518738
ensemblrs1057518738
gopubmedrs1057518738
geneviewrs1057518738
scholarrs1057518738
googlers1057518738
pharmgkbrs1057518738
gwascentralrs1057518738
openSNPrs1057518738
23andMers1057518738
23andMe allrs1057518738
SNPshotrs1057518738
SNPdbers1057518738
MSV3drs1057518738
GWAS Ctlgrs1057518738
Max Magnitude0
ClinVar
Risk rs1057518738(A;A)
Alt rs1057518738(A;A)
Reference Rs1057518738(G;G)
Significance Pathogenic
Disease Cataract 34
Variation info
Gene FOXE3
CLNDBN Cataract 34, multiple types
Reversed 0
HGVS NC_000001.10:g.47882294G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000412546.1,