Original source

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

Alleles
T/C | Ambiguity code: Y | MAF: 0.01 (C)
Location

Chromosome 17:27756922 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

This variant has 2 HGVS names - click the plus to show

About this variant

Variant displays