Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.38 (A)
Location

Chromosome 19:48978947 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 3 HGVS names - click the plus to show

About this variant

Variant displays