Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D | MAF: < 0.01 (A)
Location

Chromosome 7:140007159 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59710041

This variation has 22 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, HumanCoreExome-12, Illumina_HumanOmni5

About this variant

This variant overlaps 20 transcripts and has 3267 individual genotypes.

Variation displays