{{Rsnum
|rsid = 3731824
|Gene = ST3GAL5
|Orientation=minus
|ReferenceAllele=A
|MissenseAllele=G
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=2
|position=85861188
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Status=Merged
|Merged=1138484
|Gene_s=ST3GAL5
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 57.1 | 42.0 | 0.9
| HCB | 57.5 | 37.3 | 5.2
| JPT | 58.4 | 35.4 | 6.2
| YRI | 89.0 | 10.3 | 0.7
| ASW | 89.5 | 10.5 | 0.0
| CHB | 57.5 | 37.3 | 5.2
| CHD | 41.3 | 47.7 | 11.0
| GIH | 35.0 | 47.0 | 18.0
| LWK | 88.1 | 11.9 | 0.0
| MEX | 75.9 | 19.0 | 5.2
| MKK | 82.1 | 17.9 | 0.0
| TSI | 65.3 | 31.7 | 3.0
| HapMapRevision=28
}}{{Venter SNP
|rsid=3731824
|allele=C
|frequency=0.242
|uid=1103658153700
|type=heterozygous_SNP
|hugo=ST3GAL5
|ensembl gene=ENSG00000115525
|ensembl transcript=ENST00000306262
|sift=TOLERATED
|disease=Defects in ST3GAL5 are the cause of Amish infantile epilepsy syndrome (MIM:609056). It is an autosomal recessive disorder characterized by infantile-onset symptomatic epilepsy associated with developmental stagnation and blindness.
}}

{{GET Evidence
|gene=ST3GAL5
|aa_change=His104Arg
|aa_change_short=H104R
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs3731824
|overall_frequency_n=1697
|overall_frequency_d=10758
|overall_frequency=0.157743
|n_genomes=11
|n_genomes_annotated=0
|n_haplomes=11
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.006
|nblosum100=1
|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}}