Original source

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

Alleles
-/AA|MAF: 0.38 (-)
Location

Chromosome 10: between 62404127 and 62404128 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2513 sample genotypes.

Variant displays