Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.28 (C)
Location

Chromosome 6:111188360 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60916203

This variant has 3 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_ImmunoChip

About this variant

This variant overlaps 2 transcripts and has 2511 sample genotypes.

Variant displays