Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: 0.31 (T)
Location

Chromosome 1:16996703 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60249437

This variation has 9 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Affy GeneChip 500K

Variation displays