Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057516141

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057516141(C;G)
Make rs1057516141(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position138946552
GeneFOXL2, FOXL2NB
is asnp
is mentioned by
dbSNPrs1057516141
dbSNP (old)rs1057516141
ClinGenrs1057516141
ebirs1057516141
HLIrs1057516141
Exacrs1057516141
Gnomadrs1057516141
Varsomers1057516141
Maprs1057516141
PheGenIrs1057516141
Biobankrs1057516141
1000 genomesrs1057516141
hgdprs1057516141
ensemblrs1057516141
gopubmedrs1057516141
geneviewrs1057516141
scholarrs1057516141
googlers1057516141
pharmgkbrs1057516141
gwascentralrs1057516141
openSNPrs1057516141
23andMers1057516141
23andMe allrs1057516141
SNPshotrs1057516141
SNPdbers1057516141
MSV3drs1057516141
GWAS Ctlgrs1057516141
Max Magnitude0
ClinVar
Risk rs1057516141(G;G)
Alt rs1057516141(G;G)
Reference Rs1057516141(C;C)
Significance Pathogenic
Disease Blepharophimosis
Variation info
Gene FOXL2 FOXL2NB C3orf72
CLNDBN Blepharophimosis, ptosis, and epicanthus inversus
Reversed 1
HGVS NC_000003.11:g.138665394G>C
CLNSRC
CLNACC RCV000408854.1,