Original source

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

Alleles
G/A/C | Ancestral: G | Ambiguity code: V | MAF: 0.32 (C)
Location

Chromosome 10:69462737 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17569148

This variation has 6 HGVS names - click the plus to show

Variation displays