Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.22 (G)
Location

Chromosome 1:153261034 (forward strand) | View in location tab

Co-located

with COSMIC COSM3747558 (A/G)

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_047712

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

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni1-Quad

Variation displays