Original source

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

Alleles
CG/- | MAF: 0.31 (CG)
Location

Chromosome 5:149599130-149599131 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

Variation displays