Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.48 (G)
Location

Chromosome 4:6301627 (forward strand) | View in location tab

Co-located

with COSMIC COSM149634 (G/A) ; HGMD-PUBLIC CM000447

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

This variation has 6 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 2516 individual genotypes, is associated with 1 phenotype and is mentioned in 18 citations.

Variation displays