Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.24 (A)
Location

Chromosome 12:110915044 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

This variant has 5 HGVS names - click the plus to show

This variant has assays on 13 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts, has 6331 sample genotypes and is mentioned in 1 citation.

Variant displays