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 19:42093009 (forward strand)|View in location tab

Co-located variant

dbSNP rs58053511 (A/-)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs201249820

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 13 transcripts.

Variant displays