Original source

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

CCT/- | MAF: 0.22 (-)

Chromosome 14:100845395-100845397 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 22 HGVS names - click the plus to show

About this variant

This variant overlaps 21 transcripts and has 1092 individual genotypes.

Variation displays