Original source

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

Alleles
-/C/CC|MAF: 0.37 (C)
Location

Chromosome 11: between 2883974 and 2883975 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs375826791, rs140121791

HGVS names

This variant has 16 HGVS names - Show

About this variant

Variant displays