Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/G/T | Ancestral: C | Ambiguity code: B
Location

Chromosome 11:2159898 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM082901, CM074288

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

This variation has 24 HGVS names - click the plus to show

About this variant

This variant overlaps 26 transcripts, is associated with 4 phenotypes and is mentioned in 4 citations.

Variation displays