Original source

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

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.25 (G)

Chromosome 13:33021595 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs509751

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 2508 sample genotypes.

Variant displays