Original source

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

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

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

Most severe consequence
 
Synonymous variant
Evidence status

HGVS names

This variant has 48 HGVS names - Show

About this variant

This variant overlaps 50 transcripts and has 2545 sample genotypes.

Variant displays