Original source

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

Alleles
C/T|Ancestral: T|Ambiguity code: Y|MAF: 0.39 (C)
Location

Chromosome 19:18592963 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs56704130

HGVS names

This variant has 2 HGVS names - Show

About this variant

Variant displays