Original source

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

Alleles
-/T | MAF: 0.25 (T)
Location

Chromosome 8: between 23050293 and 23050294 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 5 HGVS names - click the plus to show

Variation displays