Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)

Chromosome 6:161785820 (forward strand) | View in location tab


with COSMIC COSM1722445 (G/A), COSM1722444 (G/A) ; HGMD-PUBLIC CM991007

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 15 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_ImmunoChip, HumanCoreExome-12

About this variant

This variant overlaps 7 transcripts, has 1093 individual genotypes, is associated with 4 phenotypes and is mentioned in 2 citations.

Variation displays