This variant has been flagged

Variation has more than 3 different alleles

Original source

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

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

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

Most severe consequence
 
5 prime UTR variant
Evidence status

HGVS names

This variant has 12 HGVS names - Show

About this variant

Variant displays