Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 19:11378233 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM980611

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_036_EPOR_133171_0006, 1760

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

About this variant

This variant overlaps 10 transcripts, 1 regulatory feature and is associated with 2 phenotypes.

Variant displays