Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A/T | Ancestral: G | Ambiguity code: D
Location

Chromosome 2:46380281 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM081583, CM080232

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11790, 11789

This variation has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts, is associated with 4 phenotypes and is mentioned in 1 citation.

Variation displays