Original source

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

Alleles
-/C | MAF: 0.48 (-)
Location

Chromosome 12: between 52794425 and 52794426 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 2 HGVS names - click the plus to show

Variation displays