Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 12:21546457 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM980968

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2283

This variation has 3 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays