Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.23 (G)
Location

Chromosome 18:5534557 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57931122, rs56424468

This variation has 15 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0, Illumina_CytoSNP12v1, Affy GeneChip 500K

About this variant

This variant overlaps 14 transcripts and has 4017 individual genotypes.

Variation displays