Original source

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

Alleles
-/CC | MAF: 0.16 (CC)
Location

Chromosome 5: between 150219564 and 150219565 (forward strand) | View in location tab

Most severe consequence

This variation has 3 HGVS names - click the plus to show

Variation displays