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 10:68989100 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM051943

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_044_KIAA1279_609367_0001, 16291

This variant has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature and is associated with 2 phenotypes.

Variant displays