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 1:169468787 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status


This variant has 2 synonyms - Show

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 2 transcripts, has 3095 sample genotypes and is associated with 1 phenotype.

Variant displays