Original source

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

Alleles
-/C/CC
Location

Chromosome 13: between 28236507 and 28236508 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 8 HGVS names - click the plus to show

Variation displays