Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: 0.14 (T)
Location

Chromosome 9:101909753 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs16918310, rs60400375

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Affy GeneChip 500K, Affy GenomeWideSNP_6.0, Illumina_CytoSNP12v1

Variation displays