Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
C/A/T | Ancestral: C | Ambiguity code: H | MAF: 0.32 (C)
Location

Chromosome 4:6304878 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_Cardio-Metabo_Chip, Illumina_HumanOmni1-Quad

Variation displays