Original source

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

Alleles
A/T|Ancestral: T|Ambiguity code: W|MAF: 0.38 (T)
Location

Chromosome 19:48978948 (forward strand)|View in location tab

Co-located variant

dbSNP rs67939886 (AT/GA)

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 3 HGVS names - Show

About this variant

Variant displays