Original source

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

Alleles
C/-|Ancestral: C|MAF: 0.25 (-)
Location

Chromosome 12:110913226 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Clinical significance

Synonyms

This variant has 4 synonyms - Show

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature, has 2505 sample genotypes, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays