Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.16 (A)
Location

Chromosome 6:6318562 (forward strand) | View in location tab

Co-located

with COSMIC COSM3762153 (C/A) ; HGMD-PUBLIC CM950376

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 9 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 5 transcripts, has 2464 individual genotypes, is associated with 4 phenotypes and is mentioned in 16 citations.

Variation displays