Original source

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

Alleles
A/T | Ambiguity code: W
Location

Chromosome 11:90055313 (forward strand) | View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs27107337

HGVS name

11:g.90055313A>T

About this variant

This variant has 45 sample genotypes.

Variant displays