Original source

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

Alleles
-/A | MAF: 0.28 (A)
Location

Chromosome 10: between 99535896 and 99535897 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

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

Variation displays