{{Rsnum
|rsid=1046974
|Gene=SAG
|Chromosome=2
|position=233346901
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.3127
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=SAG
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 14.2 | 54.0 | 31.9
| HCB | 21.2 | 46.0 | 32.8
| JPT | 7.1 | 49.6 | 43.4
| YRI | 0.0 | 2.0 | 98.0
| ASW | 1.8 | 24.6 | 73.7
| CHB | 21.2 | 46.0 | 32.8
| CHD | 15.6 | 40.4 | 44.0
| GIH | 17.8 | 43.6 | 38.6
| LWK | 0.0 | 10.0 | 90.0
| MEX | 1.8 | 45.6 | 52.6
| MKK | 0.6 | 21.2 | 78.2
| TSI | 13.7 | 52.9 | 33.3
| HapMapRevision=28
}}

{{Venter SNP
|rsid=1046974
|allele=A
|frequency=0.375
|uid=1103658396384
|type=heterozygous_SNP
|hugo=SAG
|ensembl gene=ENSG00000130561
|ensembl transcript=ENST00000252857
|sift=
|disease=Defects in SAG are the cause of Oguchi disease 1 (MIM:258100); also known as stationary night blindness Oguchi type-1. It is a form of recessively inherited stationary night blindness.
}}

{{GET Evidence
|gene=SAG
|aa_change=Val403Ile
|aa_change_short=V403I
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1046974
|overall_frequency_n=3077
|overall_frequency_d=10102
|overall_frequency=0.304593
|n_genomes=23
|n_genomes_annotated=0
|n_haplomes=28
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|genetests_testable=Y
|nblosum100=-4
|autoscore=1
|webscore=N
}}

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