Original source

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

Alleles
C/A/T | Ancestral: C | Ambiguity code: H | MAF: 0.41 (T)
Location

Chromosome 3:98816974 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1660054, rs58347474

This variation has 14 HGVS names - click the plus to show

Variation displays