Original source

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

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

Chromosome 11:6615442 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM990373

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

Uniprot VAR_009610

This variant has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 32 transcripts, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays