Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: < 0.01 (T)
Location

Chromosome 12:11648492 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs68022412

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2505 sample genotypes.

Variant displays