Original source

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

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

Chromosome 11:17470119 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM061628, CM072823

Most severe consequence
Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

This variation has 16 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts, is associated with 5 phenotypes and is mentioned in 7 citations.

Variation displays