Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.18 (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_HumanOmni1-Quad, Illumina_ExomeChip

About this variant

This variant overlaps 2 transcripts and has 2508 individual genotypes.

Variation displays