Original source

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

Alleles
G/A|Ambiguity code: R|MAF: 0.01 (A)
Location

Chromosome 10:77974715 (forward strand)|View in location tab

Co-located variant

dbSNP rs367810633 (G/-)

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

Variant displays