Original source

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

Alleles
TC/-
Location

Chromosome 12:43757176-43757177 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 21 transcripts.

Variant displays