Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.48 (G)
Location

Chromosome 22:35072496 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60493943, rs60643890

This variation has 3 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Affy GeneChip 500K, Illumina_Human660W-quad, Affy GenomeWideSNP_6.0

Variation displays