Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.31 (A)
Location

Chromosome 11:44608755 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 8 HGVS names - click the plus to show

Variation displays