Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

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

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

Most severe consequence
Synonymous variant
Evidence status


Archive dbSNP rs59710041

HGVS names

This variant has 38 HGVS names - Show

Genotyping chips

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

About this variant

This variant overlaps 20 transcripts and has 3267 sample genotypes.

Variant displays