Original source

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

Alleles
A/T|Ancestral: A|Ambiguity code: W
Location

Chromosome 19:42089761 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs3203554, rs16975674

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 11 transcripts.

Variant displays