Original source

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

T/- | Ancestral: T

Chromosome 8:23059684 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 4 sample genotypes.

Variant displays