Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
Intron variant
Evidence status


Archive dbSNP rs116983777, rs1656080

HGVS names

This variant has 14 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 18 transcripts, has 2591 sample genotypes and is mentioned in 1 citation.

Variant displays