This variant has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
A/C/G/T | Ambiguity code: N | MAF: 0.37 (A)
Location

Chromosome 11:18402940 (forward strand) | View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

This variant has 51 HGVS names - click the plus to show

About this variant

This variant overlaps 75 transcripts and has 2512 sample genotypes.

Variant displays