Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 12:42469523 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM085653

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 15752, NM_153026.2:c.311G>A

This variation has 17 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12

Variation displays