Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.06 (G)
Location

Chromosome 17:63918836 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57952803

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

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_Human660W-quad

About this variant

This variant overlaps 8 transcripts, has 2508 individual genotypes and is mentioned in 1 citation.

Variation displays