Original source

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

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

Chromosome 9:122226302 (forward strand) | View in location tab

Most severe consequence
Intron variant
HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 269 sample genotypes.

Variant displays