Original source

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

T/G | Ancestral: G | Ambiguity code: K | MAF: 0.41 (T)

Chromosome 7:100824547 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
Evidence status


Archive dbSNP rs1656081

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 9 transcripts, has 3693 sample genotypes and is mentioned in 1 citation.

Variant displays