Original source

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

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

Chromosome 17:26727722 (forward strand) | View in location tab

Co-located

with dbSNP rs200596790 (A/G)

Most severe consequence
Evidence status

This variation has 12 HGVS names - click the plus to show

Variation displays