Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.34 (C)
Location

Chromosome 10:135343738 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58926648

This variation has 9 HGVS names - click the plus to show

This variation has assays on 8 chips - click the plus to show

Variation displays