Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.40 (C)

Chromosome 12:6535615 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs56744165

HGVS names

This variant has 10 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 28 transcripts, 1 regulatory feature, has 4009 sample genotypes and is mentioned in 3 citations.

Variant displays