Original source

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

Alleles
AAG/-|MAF: 0.09 (-)
Location

Chromosome 16:50740428-50740430 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs147231230, rs375701330

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 14 transcripts and has 2506 sample genotypes.

Variant displays