Original source

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

Alleles
A/T | Ambiguity code: W
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs27107337

HGVS name

11:g.90055313A>T

Variation displays