Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | [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

Variation displays