Original source

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

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

Chromosome 12:21657972 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs1677123, rs60681437

HGVS names

This variant has 3 HGVS names - Show

About this variant

Variant displays