Original source

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

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

Chromosome 2:231513520 (forward strand) | View in location tab

Most severe consequence
Splice region variant
Evidence status


Archive dbSNP rs59272379

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 1 transcript, has 3769 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays