Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.45 (A)
Location

Chromosome 10:99533711 (forward strand) | View in location tab

Co-located

with dbSNP rs200965740 (A/-)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60567633

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

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays