Original source

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

Alleles
A/- | Ancestral: A | MAF: < 0.01 (A)
Location

Chromosome 17:28400706 (forward strand) | View in location tab

Co-located

with dbSNP rs200596790 (A/G), rs201732528 (A/T)

Most severe consequence
Evidence status

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

Variation displays