Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D
Location

Chromosome 1:149321645 (forward strand) | View in location tab

Co-located

with COSMIC COSM329521 (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NC_000001.9:g.143787132G>A

This variation has 4 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays