Original source

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

Alleles
CT/-|MAF: < 0.01 (-)
Location

Chromosome 5:171388761-171388762 (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

Variant displays