Original source

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

Alleles
A/- | Ancestral: A | MAF: 0.23 (A)
Location

Chromosome 16:74720167 (forward strand) | View in location tab

Co-located

with dbSNP rs74250246 (A/T)

Most severe consequence

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

Variation displays