Original source

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

Alleles
-/C | MAF: 0.19 (-)
Location

Chromosome 20: between 59310828 and 59310829 (forward strand) | View in location tab

Most severe consequence

This variation has 6 HGVS names - click the plus to show

Variation displays