Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 11:114082115 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs10750049, rs58465618

This variation has 5 HGVS names - click the plus to show

This variation has assays on 7 chips - click the plus to show

Variation displays