Original source

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

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.05 (G)

Chromosome 2:219252322 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 24 transcripts and has 2589 sample genotypes.

Variant displays