Original source

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

CT/- | MAF: 0.19 (-)

Chromosome 16:28882404-28882405 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs71856485, rs146965224

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 2505 sample genotypes.

Variant displays