Original source

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

Alleles
A/G | Ambiguity code: R | MAF: 0.22 (A)
Location

Chromosome 6:32642684 (forward strand) | View in location tab

Co-located

with dbSNP rs35029979 (A/G)

Most severe consequence
Evidence status

This variation has 10 synonyms - click the plus to show

This variation has 10 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni1-Quad

Variation displays