Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

ACAAA/- | MAF: 0.24 (-)

Chromosome 16:50752262-50752266 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs151087977

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 13 transcripts and has 2508 sample genotypes.

Variant displays