Original source

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

A/- | Ancestral: A | MAF: 0.38 (-)

Chromosome 12:21910318 (forward strand) | View in location tab

Most severe consequence
Splice region variant
Evidence status

Clinical significance


This variant has 4 synonyms - Show

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 5 transcripts, has 2510 sample genotypes and is associated with 1 phenotype.

Variant displays