Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.06 (T)
Location

Chromosome 6:111928920 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs4541778

HGVS name

6:g.111928920C>T

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

Variation displays