Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.35 (C)

Chromosome 14:102047890 (forward strand) | View in location tab


with COSMIC COSM147844 (T/C)

Most severe consequence
Evidence status

Clinical significance

This variation has 6 HGVS names - click the plus to show

This variation has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts, has 4399 individual genotypes and is associated with 1 phenotype.

Variation displays