Original source

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

Alleles
C/G/T | Ambiguity code: B | MAF: < 0.01 (G)
Location

Chromosome 12:52287578 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 10 HGVS names - click the plus to show

About this variant

Variant displays