Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.46 (T)
Location

Chromosome 15:89398605 (forward strand) | View in location tab

Co-located

with COSMIC COSM146361 (G/T)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs52808766, rs59582752

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

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

Variation displays