Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.02 (T)
Location

Chromosome 21:43809092 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM054156

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11613314

This variation has 13 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays