Original source

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

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

Chromosome 16:31191418 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM091086, CM104702, CM091090

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 22 HGVS names - click the plus to show

About this variant

This variant overlaps 24 transcripts and is associated with 4 phenotypes.

Variation displays