Original source

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

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

Chromosome 6:111607717 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs4541778

HGVS name

6:g.111607717C>T

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

Variation displays