Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.05 (C)
Location

Chromosome 9:104194053 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17187052, rs1634125

This variation has 2 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0, Illumina_1M-duo, Illumina_HumanOmni5

Variation displays