Original source

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

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

Chromosome 16:20348652 (forward strand) | View in location tab


with HGMD-PUBLIC CM023184, CM034987

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 18 HGVS names - click the plus to show

About this variant

This variant overlaps 25 transcripts and is associated with 5 phenotypes.

Variation displays