Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.45 (T)
Location

Chromosome 6:151622842 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

6:g.151622842C>T

Genotyping chips

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

Variation displays