Table 2. Detailed information of ALDH7A1 SNPs from dbSNP.

dbSNP	rs13182402	rs12659017
Organism	Homo sapiens	Homo sapiens
Position1	chr5:126582456	chr5:126652483
Nucleotide change	A>G	G>A
Variation type	SNV	SNV
Minor allele frequency2	G = 0.0575	A = 0.7044
Gene consequence	Intron variant	None
Clinical significance	Not reported in ClinVar	Not reported in ClinVar

¹GRCh38.p12. ²Minor allele frequency using the East Asian population from 1000 Genomes.