Original source

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

Alleles
C/A/T | Ancestral: G | Ambiguity code: H | MAF: 0.02 (T)
Location

Chromosome 13:102845721 (forward strand) | View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

This variant has 8 HGVS names - click the plus to show

About this variant

Variant displays