Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.47 (C)
Location

Chromosome 9:286593 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 6 synonyms - click the plus to show

This variation has 22 HGVS names - click the plus to show

This variation has assays on 9 chips - click the plus to show

Variation displays