Original source

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

Alleles
G/C | Ambiguity code: S
Location

Chromosome 11:90055263 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.90055263G>C

About this variant

This variant has 28 individual genotypes.

Variation displays