Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.26 (C)
Location

Chromosome 17:17237171 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57111798, rs16961462

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 10 transcripts, has 2828 individual genotypes and is mentioned in 1 citation.

Variation displays