Original source

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

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

Chromosome 12:120437284 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

12:g.120437284T>C

About this variant

This variant overlaps 4 transcripts and has 7 sample genotypes.

Variant displays