Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

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

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

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs60916203

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ImmunoChip

About this variant

This variant overlaps 2 transcripts and has 2581 sample genotypes.

Variant displays