Original source

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

Alleles
-/C | MAF: < 0.01 (C)
Location

Chromosome 15: between 66384940 and 66384941 (forward strand) | View in location tab

Most severe consequence

This variation has 6 HGVS names - click the plus to show

Variation displays