Original source

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

Alleles
CT/-|MAF: 0.19 (-)
Location

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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