Original source

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

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

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

Co-located

with HGMD-PUBLIC CS045643

Most severe consequence
Evidence status

Clinical significance

Synonyms

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

Variation displays