Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 11:2159883 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM082900

Most severe consequence
Evidence status

Clinical significance

Synonyms

Uniprot VAR_063739

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

About this variant

This variant overlaps 13 transcripts, is associated with 2 phenotypes and is mentioned in 1 citation.

Variation displays