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 | MAF: 0.16 (T)
Location

Chromosome 3:129059034 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60499754

HGVS name

3:g.129059034T>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Affy GenomeWideSNP_6.0, Illumina_HumanOmni5

Variation displays