Original source

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

C/A/T|Ancestral: A|Ambiguity code: H|MAF: 0.32 (C)

Chromosome 8:22162781 (forward strand)|View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs59217304, rs2234822

HGVS names

This variant has 18 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 48 transcripts, has 3742 sample genotypes and is mentioned in 1 citation.

Variant displays