Original source

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

Alleles
-/C|MAF: 0.32 (C)
Location

Chromosome 19: between 48970229 and 48970230 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 3 HGVS names - Show

About this variant

Variant displays