Original source

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

-/GT | MAF: 0.02 (GT)

Chromosome 8: between 127413855 and 127413856 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2504 sample genotypes.

Variant displays