Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.21 (T)
Location

Chromosome 11:45953579 (forward strand) | View in location tab

Co-located

with COSMIC COSM3752368 (C/T), COSM3752369 (C/T)

Most severe consequence
Evidence status

This variation has 4 synonyms - click the plus to show

This variation has 8 HGVS names - click the plus to show

This variation has assays on 12 chips - click the plus to show

Variation displays