Original source

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

AAG/- | MAF: 0.09 (-)

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

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs147231230, rs375701330

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

About this variant

This variant overlaps 14 transcripts and has 2506 sample genotypes.

Variant displays