Original source

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

A/C/G | Ancestral: A | Ambiguity code: V | MAF: 0.04 (G)

Chromosome 6:160707855 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
Evidence status


Archive dbSNP rs1652509

HGVS names

This variant has 20 HGVS names - Show

About this variant

This variant overlaps 18 transcripts and has 2505 sample genotypes.

Variant displays