Original source

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

Alleles
A/-
Location

Chromosome 12:52287337 (forward strand)|View in location tab

Co-located variant

dbSNP rs751721656 (A/G)

Most severe consequence
 
Intron variant
HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and 2 regulatory features.

Variant displays