Original source

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

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

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