Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.33 (T)
Location

Chromosome 13:27623299 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

This variation has assays on 13 chips - click the plus to show

About this variant

This variant overlaps 11 transcripts, has 4255 individual genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variation displays