Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 3:185507961 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3188875

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

Genotyping chips

This variation has assays on: Illumina_Human1M-duo

Variation displays