{{Rsnum
|rsid=1208285
|Gene=MIR4520A
|Chromosome=6
|position=133837662
|Orientation=plus
|GMAF=0.2842
|Gene_s=MIR4520A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 16.8 | 42.5 | 40.7
| HCB | 29.9 | 50.4 | 19.7
| JPT | 23.9 | 42.5 | 33.6
| YRI | 0.7 | 2.7 | 96.6
| ASW | 1.8 | 19.3 | 78.9
| CHB | 29.9 | 50.4 | 19.7
| CHD | 21.1 | 52.3 | 26.6
| GIH | 15.8 | 40.6 | 43.6
| LWK | 0.0 | 6.4 | 93.6
| MEX | 5.2 | 48.3 | 46.6
| MKK | 0.0 | 7.7 | 92.3
| TSI | 14.7 | 37.3 | 48.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22306654
|Trait=None
|Title=Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis.
|RiskAllele=C
|Pval=6E-7
|OR=1.2500
|ORtxt=None
|OA=1
}}

{{GET Evidence
|gene=BC032958
|aa_change=Ile125Thr
|aa_change_short=I125T
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1208285
|overall_frequency_n=23
|overall_frequency_d=108
|overall_frequency=0.212963
|n_genomes=10
|n_genomes_annotated=0
|n_haplomes=13
|n_articles=0
|n_articles_annotated=0
|nblosum100=3
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}