Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.36 (C)
Location

Chromosome 5:126544897 (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: HumanCoreExome-12, Illumina_HumanOmni5

About this variant

This variant overlaps 6 transcripts, has 2540 individual genotypes and is mentioned in 1 citation.

Variation displays