Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.25 (A)
Location

Chromosome 12:53721840 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]
Evidence status

Synonyms

Archive dbSNP rs17102164, rs2293443

This variation has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 20 transcripts and has 2762 individual genotypes.

Variation displays