Original source

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

Alleles
C/G/T | Ancestral: C | Ambiguity code: B | MAF: < 0.01 (T)
Location

Chromosome 11:17397055 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS951534

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NM_000352.3:c.3989-9G>A

This variant has 18 HGVS names - click the plus to show

About this variant

This variant overlaps 22 transcripts, has 2504 sample genotypes and is associated with 3 phenotypes.

Variant displays