Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.37 (C)
Location

Chromosome 11:636784 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR994758

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3824859

HGVS name

11:g.636784T>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni2.5

Variation displays