Original source

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

Alleles
C/G | Ambiguity code: S | MAF: 0.34 (C)
Location

Chromosome 6:160753839 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1782612, rs60909505

HGVS name

6:g.160753839C>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5, Illumina_1M-duo

Variation displays