Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 3 HGVS names - click the plus to show

About this variant

Variant displays