Original source

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

C/G/T | Ancestral: G | Ambiguity code: B | MAF: 0.09 (G)

Chromosome 7:100823256 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs116983777, rs1656080

This variation has 14 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 18 transcripts, has 1183 individual genotypes and is mentioned in 1 citation.

Variation displays