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rs1057518737

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518737(C;G)
Make rs1057518737(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position47416666
GeneFOXE3, LINC01389
is asnp
is mentioned by
dbSNPrs1057518737
dbSNP (old)rs1057518737
ClinGenrs1057518737
ebirs1057518737
HLIrs1057518737
Exacrs1057518737
Gnomadrs1057518737
Varsomers1057518737
LitVarrs1057518737
Maprs1057518737
PheGenIrs1057518737
Biobankrs1057518737
1000 genomesrs1057518737
hgdprs1057518737
ensemblrs1057518737
gopubmedrs1057518737
geneviewrs1057518737
scholarrs1057518737
googlers1057518737
pharmgkbrs1057518737
gwascentralrs1057518737
openSNPrs1057518737
23andMers1057518737
23andMe allrs1057518737
SNPshotrs1057518737
SNPdbers1057518737
MSV3drs1057518737
GWAS Ctlgrs1057518737
Max Magnitude0
ClinVar
Risk rs1057518737(G;G)
Alt rs1057518737(G;G)
Reference Rs1057518737(C;C)
Significance Pathogenic
Disease Cataract 34
Variation info
Gene FOXE3
CLNDBN Cataract 34, multiple types
Reversed 0
HGVS NC_000001.10:g.47882338C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000412651.1,