Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has assays on 5 chips - click the plus to show

About this variant

Variant displays