Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.04 (T)
Location

Chromosome 4:120055009 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

4:g.120055009C>T

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0, Illumina_1M-duo, Illumina_HumanOmni5

Variation displays