Original source

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

Alleles
G/- | Ancestral: T | MAF: 0.33 (G)
Location

Chromosome 10:119662226 (forward strand) | View in location tab

Co-located

with dbSNP rs2736423 (G/T)

Most severe consequence

This variation has 3 HGVS names - click the plus to show

Variation displays