Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 16:20359974 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM034987, CM023184

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 26 HGVS names - click the plus to show

Variation displays