Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M|MAF: 0.26 (A)
Location

Chromosome 19:48393986 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs57555058, rs1799276

HGVS name

19:g.48393986C>A

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

Variant displays