Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 11:6391976 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920624

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 15098

This variation has 15 HGVS names - click the plus to show

About this variant

This variant overlaps 27 transcripts and is associated with 2 phenotypes.

Variation displays