Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)
Location

Chromosome 1:17323602 (forward strand) | View in location tab

Co-located

with COSMIC COSM108065 (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NC_000001.9:g.17196189G>A

This variation has 12 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Somatic mutation displays