Original source

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

C/G | Ancestral: C | Ambiguity code: S | MAF: 0.28 (C)

Chromosome 4:6293966 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

Clinical significance


This variant has 2 synonyms - Show

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip

About this variant

This variant overlaps 5 transcripts, has 2783 sample genotypes, is associated with 3 phenotypes and is mentioned in 10 citations.

Variant displays