Original source

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

Alleles
T/A/C/G | Ancestral: T | Ambiguity code: N
Location

Chromosome 14:24259950 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM013051

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5807

This variation has 15 HGVS names - click the plus to show

About this variant

This variant overlaps 28 transcripts and is associated with 2 phenotypes.

Variation displays