Original source

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

AC/- | MAF: 0.47 (-)

Chromosome 12:20833670-20833671 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs140550860

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

About this variant

This variant overlaps 5 transcripts and has 1094 individual genotypes.

Variation displays