Original source

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

-/CTC | MAF: 0.20 (CTC)

Chromosome 22: between 50578777 and 50578778 (forward strand) | View in location tab

Most severe consequence

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

About this variant

This variant overlaps 28 transcripts and has 1092 individual genotypes.

Variation displays