Have questions? Visit https://www.reddit.com/r/SNPedia

rs672601295

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs672601295(A;A)
Make rs672601295(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position86510985
GeneFOXF1
is asnp
is mentioned by
dbSNPrs672601295
ebirs672601295
HLIrs672601295
Exacrs672601295
Varsomers672601295
Maprs672601295
PheGenIrs672601295
hapmaprs672601295
1000 genomesrs672601295
hgdprs672601295
ensemblrs672601295
gopubmedrs672601295
geneviewrs672601295
scholarrs672601295
googlers672601295
pharmgkbrs672601295
gwascentralrs672601295
openSNPrs672601295
23andMers672601295
23andMe allrs672601295
SNP Nexus

SNPshotrs672601295
SNPdbers672601295
MSV3drs672601295
GWAS Ctlgrs672601295
Max Magnitude0
ClinVar
Risk rs672601295(A;A)
Alt rs672601295(A;A)
Reference rs672601295(G;G)
Significance Probable-Pathogenic
Disease Pyloric stenosis
Variation info
Gene FOXF1
CLNDBN Pyloric stenosis, infantile hypertrophic, 5
Reversed 0
HGVS NC_000016.9:g.86544591G>A
CLNSRC
CLNACC RCV000119307.1,