Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.04 (G)
Location

Chromosome 1:145925876 (forward strand) | View in location tab

Co-located

with dbSNP rs77434912 (G/C)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays