Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 4 synonyms - click the plus to show

This variant has 6 HGVS names - click the plus to 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