Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Co-located

with dbSNP rs58053511 (A/-)

Most severe consequence
Synonyms

Archive dbSNP rs201249820

This variation has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts.

Variation displays