Original source

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

Alleles
CT/- | MAF: 0.01 (-)
Location

Chromosome 5:171388761-171388762 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 11 HGVS names - click the plus to show

Variation displays