Original source

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

Alleles
G/- | Ancestral: G | MAF: 0.42 (-)
Location

Chromosome 8:93921096 (forward strand) | View in location tab

Co-located

with dbSNP rs201669269 (G/A)

Most severe consequence
Evidence status

This variation has 11 HGVS names - click the plus to show

Variation displays