Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 11:6617040 (forward strand) | View in location tab

Co-located

with COSMIC COSM3718418 (G/A) ; HGMD-PUBLIC CM970326

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 15415

This variation has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 24 transcripts and is associated with 2 phenotypes.

Variation displays