Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)
Location

Chromosome 11:27658560 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM023769

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

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

This variation has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 27 transcripts, has 2541 individual genotypes, is associated with 3 phenotypes and is mentioned in 3 citations.

Variation displays