Original source

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

-/A/AA | MAF: 0.40 (-)

Chromosome 1: between 225420309 and 225420310 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2508 sample genotypes.

Variant displays