Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/G/T | Ancestral: G | Ambiguity code: B | MAF: 0.15 (T)
Location

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs116983777, rs1656080

This variant has 14 HGVS names - click the plus to 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