Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.18 (T)
Location

Chromosome 15:38351373 (forward strand) | View in location tab

Co-located

with COSMIC COSM3999508 (T/C)

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

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

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

Variation displays