Original source

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

Alleles
AA/-|MAF: 0.35 (AA)
Location

Chromosome 19:16486620-16486621 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs373470899

HGVS names

This variant has 6 HGVS names - Show

About this variant

Variant displays