Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.20 (T)
Location

Chromosome 11:27658369 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM020369

Most severe consequence
Evidence status

Clinical significance

This variation has 8 synonyms - click the plus to show

This variation has 44 HGVS names - click the plus to show

This variation has assays on 15 chips - click the plus to show

About this variant

This variant overlaps 27 transcripts, has 2642 individual genotypes, is associated with 11 phenotypes and is mentioned in 348 citations.

Variation displays