Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.12 (A)
Location

Chromosome 10:6045063 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60127900

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

This variation has assays on 12 chips - click the plus to show

Variation displays