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rs1057518868

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518868(A;T)
Make rs1057518868(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position86510849
GeneFENDRR, FOXF1
is asnp
is mentioned by
dbSNPrs1057518868
dbSNP (old)rs1057518868
ClinGenrs1057518868
ebirs1057518868
HLIrs1057518868
Exacrs1057518868
Gnomadrs1057518868
Varsomers1057518868
LitVarrs1057518868
Maprs1057518868
PheGenIrs1057518868
Biobankrs1057518868
1000 genomesrs1057518868
hgdprs1057518868
ensemblrs1057518868
gopubmedrs1057518868
geneviewrs1057518868
scholarrs1057518868
googlers1057518868
pharmgkbrs1057518868
gwascentralrs1057518868
openSNPrs1057518868
23andMers1057518868
23andMe allrs1057518868
SNPshotrs1057518868
SNPdbers1057518868
MSV3drs1057518868
GWAS Ctlgrs1057518868
Max Magnitude0
ClinVar
Risk rs1057518868(T;T)
Alt rs1057518868(T;T)
Reference Rs1057518868(A;A)
Significance Probable-Pathogenic
Disease Fetal megacystis Urethral atresia Ventricular septal defect
Variation info
Gene FENDRR FOXF1
CLNDBN Fetal megacystis Urethral atresia Ventricular septal defect
Reversed 0
HGVS NC_000016.9:g.86544455A>T
CLNSRC
CLNACC RCV000415110.1,