Original source

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

Alleles
G/A/C | Ancestral: G | Ambiguity code: V
Location

Chromosome 12:109784379 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM106801, CM106802

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 33469, 33470

This variation has 34 HGVS names - click the plus to show

About this variant

This variant overlaps 16 transcripts and is associated with 4 phenotypes.

Variation displays