Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
TC/- | MAF: 0.02 (-)
Location

Chromosome 12:43757176-43757177 (forward strand) | View in location tab

Most severe consequence

This variation has 10 HGVS names - click the plus to show

Variation displays