This variation has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/A/G/T | Ancestral: C | Ambiguity code: N | MAF: 0.35 (C)
Location

Chromosome 4:6303151 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 9 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip, Illumina_Human1M-duo, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 15 transcripts and has 2769 individual genotypes.

Variation displays