Original source

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

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

Chromosome 12:11688107-11688108 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 6 HGVS names - Show

About this variant

Variant displays