Original source

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

A/T | Ancestral: A | Ambiguity code: W

Chromosome 18:5405834 (forward strand) | View in location tab

Most severe consequence
Intron variant
HGVS names

This variant has 17 HGVS names - Show

About this variant

This variant overlaps 17 transcripts and has 1 sample genotype.

Variant displays