Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)
Location

Chromosome 21:42383216 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]
Evidence status

Clinical significance

Synonyms

LSDB 18214966

This variation has 8 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Affy GenomeWideSNP_6.0, Illumina_HumanOmni5

Variation displays