Original source

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

G/A | Ancestral: A | Ambiguity code: R | MAF: 0.22 (G)

Chromosome 7:155461298 (forward strand) | View in location tab


with HGMD-PUBLIC CS045643

Most severe consequence
Evidence status

Clinical significance


Archive dbSNP rs60350369, rs3808334

This variation has 2 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 2 transcripts, has 1116 individual genotypes, is associated with 2 phenotypes and is mentioned in 15 citations.

Variation displays