Original source

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

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

Chromosome 12:52469290 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 3 transcripts.

Variant displays