Original source

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

A/G/T|Ancestral: G|Ambiguity code: D|MAF: 0.41 (G)

Chromosome 12:6535556 (forward strand)|View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs116947349, rs59307765

HGVS names

This variant has 20 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 56 transcripts, 1 regulatory feature, has 2510 sample genotypes and is mentioned in 4 citations.

Variant displays