Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.27 (T)
Location

Chromosome 10:124215421 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58200861

This variation has 2 HGVS names - click the plus to show

10:g.124215421C>T
ENST00000528446.1:c.297+881C>T

This variation has assays on 7 chips - click the plus to show

Variation displays