Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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 variant

dbSNP rs200653150 (C/-)

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 8 HGVS names - Show

About this variant

Variant displays