Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.02 (C)
Location

Chromosome 6:118548260 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR082029

Most severe consequence
 
Intron variant
Evidence status

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

About this variant

Variant displays