Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.25 (T)
Location

Chromosome 12:52468473 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

12:g.52468473C>T

About this variant

This variant overlaps 3 transcripts and has 2579 sample genotypes.

Variant displays