Original source

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

T/A | Ancestral: T | Ambiguity code: W | MAF: < 0.01 (A)

Chromosome 16:23614142 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

Clinical significance


This variant has 4 synonyms - Show

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 5 transcripts, has 2783 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays