Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.01 (C)
Location

Chromosome 13:28064234 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59330145

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

Variation displays