Original source

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

Alleles
C/A/G/T | Ancestral: C | Ambiguity code: N
Location

Chromosome 6:6151813 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS920751

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 1817

This variation has 9 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12

About this variant

This variant overlaps 3 transcripts and is associated with 2 phenotypes.

Variation displays