Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.13 (C)
Location

Chromosome 9:121313007 (forward strand) | View in location tab

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

Synonyms

Archive dbSNP rs406935, rs60890758

This variation has 14 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

Variation displays