Original source

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

Alleles
C/A | Ambiguity code: M | MAF: 0.44 (C)
Location

Chromosome 12:49265973 (forward strand) | View in location tab

Co-located

with dbSNP rs200653150 (C/-)

Most severe consequence
 
Intron variant
Evidence status

This variant has 8 HGVS names - click the plus to show

About this variant

Variant displays