Original source

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

G/T | Ancestral: T | Ambiguity code: K

Chromosome 8:42455259 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 1 sample genotype.

Variant displays