Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.49 (C)
Location

Chromosome 9:75303653 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

This variation has 4 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

Variation displays