Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

A/- | Ancestral: A

Chromosome 20:53566987 (forward strand) | View in location tab


with dbSNP rs74838016 (A/C)

Most severe consequence
Intron variant

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

About this variant

This variant overlaps 4 transcripts and has 7 sample genotypes.

Variant displays