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rs752504125

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs752504125(A;A)
Make rs752504125(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position86511227
GeneFOXF1
is asnp
is mentioned by
dbSNPrs752504125
ebirs752504125
HLIrs752504125
Exacrs752504125
Varsomers752504125
Maprs752504125
PheGenIrs752504125
hapmaprs752504125
1000 genomesrs752504125
hgdprs752504125
ensemblrs752504125
gopubmedrs752504125
geneviewrs752504125
scholarrs752504125
googlers752504125
pharmgkbrs752504125
gwascentralrs752504125
openSNPrs752504125
23andMers752504125
23andMe allrs752504125
SNP Nexus

SNPshotrs752504125
SNPdbers752504125
MSV3drs752504125
GWAS Ctlgrs752504125
Max Magnitude0
ClinVar
Risk rs752504125(A;A)
Alt rs752504125(A;A)
Reference rs752504125(G;G)
Significance Probable-Pathogenic
Disease VATER association
Variation info
Gene FOXF1
CLNDBN VATER association
Reversed 0
HGVS NC_000016.9:g.86544833G>T
CLNSRC
CLNACC RCV000201858.1,