Original source

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

AAG/- | MAF: 0.01 (-)

Chromosome 17:58985895-58985897 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs372161170, rs140588752

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2504 sample genotypes.

Variant displays