Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.07 (A)
Location

Chromosome 19:5830588 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

19:g.5830588G>A

About this variant

This variant overlaps 12 transcripts and has 2506 sample genotypes.

Variant displays