Original source

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

Alleles
A/C|Ancestral: A|Ambiguity code: M|MAF: 0.11 (C)
Location

Chromosome 19:42087952 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs386518669

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

Variant displays