Original source

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

G/A/C | Ancestral: G | Ambiguity code: V | MAF: 0.04 (A)

Chromosome 1:236755183 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


This variant has 2 synonyms - Show

HGVS names

This variant has 16 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 8 transcripts, has 2539 sample genotypes, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays