Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.31 (T)

Chromosome 20:45919554 (forward strand) | View in location tab

Most severe consequence
Regulatory region variant
Evidence status

Clinical significance


This variant has 2 synonyms - Show

HGVS name


Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 1 regulatory feature, has 2510 sample genotypes, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays