Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.11 (C)
Location

Chromosome 12:11687466 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs364818, rs58265938

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

About this variant

This variant overlaps 4 transcripts and has 2773 sample genotypes.

Variant displays