Original source

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

Alleles
-/CT | MAF: 0.43 (-)
Location

Chromosome 17: between 63498093 and 63498094 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60243473, rs143875197

This variation has 4 HGVS names - click the plus to show

Variation displays