Original source

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

Alleles
T/C/G|Ancestral: C|Ambiguity code: B|MAF: 0.32 (T)
Location

Chromosome 17:64321170 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs386421216, rs117480038

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

Variant displays