Original source

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

Alleles
AGGGATGGTGGCACC/- | MAF: 0.46 (-)
Location

Chromosome 5:174725599-174725613 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

About this variant

This variant overlaps 2 transcripts and has 2505 individual genotypes.

Variation displays