Original source

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

-/AAG | MAF: 0.22 (AAG)

Chromosome 8: between 27809764 and 27809765 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 2509 individual genotypes.

Variation displays