Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M
Location

Chromosome 12:6840746 (forward strand) | View in location tab

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

Archive dbSNP rs386503888

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 21 transcripts and has 1 individual genotype.

Variation displays