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 | MAF: < 0.01 (C)
Location

Chromosome 11:72079093 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 16 HGVS names - click the plus to show

Variation displays