Original source

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

G/A | Ancestral: A | Ambiguity code: R | MAF: 0.28 (G)

Chromosome 6:52439192 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs61307565

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 4 transcripts, has 3856 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays