Original source

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

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.02 (G)

Chromosome 1:186676537 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status


Archive dbSNP rs4134746, rs2230031

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 6 transcripts, has 3504 sample genotypes and is mentioned in 1 citation.

Variant displays