Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 15:88855374 (forward strand) | View in location tab


with COSMIC COSM3927718 (G/T), COSM146361 (G/T)

Most severe consequence
Evidence status


Archive dbSNP rs52808766, rs59582752

This variation has 11 HGVS names - click the plus to show

This variation has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts and has 2438 individual genotypes.

Variation displays