Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M|MAF: 0.01 (A)
Location

Chromosome 12:48771159 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and has 2773 sample genotypes.

Variant displays