Original source

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

Alleles
A/C/G | Ancestral: A | Ambiguity code: V
Location

Chromosome 11:17470119 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM072823, CM061628

Most severe consequence
Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

This variation has 16 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts, is associated with 5 phenotypes and is mentioned in 6 citations.

Variation displays