Original source

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

Alleles
T/- | Ancestral: T | MAF: 0.27 (-)
Location

Chromosome 16:74736059 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs141975099, rs373932135

This variation has 4 HGVS names - click the plus to show

Variation displays