Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.43 (T)

Chromosome 1:231395881 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs56654310

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 2 transcripts, 1 regulatory feature, has 3762 sample genotypes and is mentioned in 6 citations.

Variant displays