Original source

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

Alleles
CTC/- | MAF: 0.09 (-)
Location

Chromosome 13:27644768-27644770 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs147271649

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

Variation displays