Original source

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

Alleles
C/G | Ancestral: A | Ambiguity code: S | MAF: 0.39 (C)
Location

Chromosome 20:9072909 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 5 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Affy GeneChip 500K, Affy GenomeWideSNP_6.0

About this variant

This variant overlaps 4 transcripts and has 4610 individual genotypes.

Variation displays