Original source

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

Alleles
A/C|Ancestral: C|Ambiguity code: M|MAF: 0.37 (A)
Location

Chromosome 19:844077 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs643029

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5

About this variant

Variant displays