Original source

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

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

Chromosome 22:36300203 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 4 transcripts, has 72 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays