Original source

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

A/C | Ancestral: A | Ambiguity code: M | MAF: 0.04 (C)

Chromosome 18:22168857 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2505 sample genotypes.

Variant displays