Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.42 (A)
Location

Chromosome 1:88682820 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 2 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0, Affy GeneChip 500K, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 6 transcripts and has 3927 individual genotypes.

Variation displays