Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 19:41985082 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM042304

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5378, NM_152296.3:c.829G>A

This variation has 14 HGVS names - click the plus to show

About this variant

This variant overlaps 9 transcripts, is associated with 1 phenotype and is mentioned in 2 citations.

Variation displays