Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.12 (T)

Chromosome 21:42389975 (forward strand) | View in location tab


with COSMIC COSM4002040 (C/A), COSM4002043 (C/T), COSM4002045 (C/T), COSM4002042 (C/A), COSM4002044 (C/T), COSM4002041 (C/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

This variation has 10 HGVS names - click the plus to show

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

About this variant

This variant overlaps 6 transcripts, has 2656 individual genotypes, is associated with 1 phenotype and is mentioned in 3 citations.

Variation displays