Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.03 (A)
Location

Chromosome 12:11687483 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58125931, rs399828

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 2510 sample genotypes.

Variant displays