Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57931122, rs56424468

HGVS names

This variant has 15 HGVS names - Show

Genotyping chips

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

About this variant

This variant overlaps 14 transcripts and has 4017 sample genotypes.

Variant displays