Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 12:7693321 (forward strand) | View in location tab

Most severe consequence
 
Intron variant

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript.

Variant displays