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: 0.36 (T)

Chromosome 1:16987159 (forward strand) | View in location tab


with COSMIC COSM3750608 (C/T), COSM3750609 (C/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 7 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni2.5

About this variant

This variant overlaps 8 transcripts, has 1103 individual genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variation displays