Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 11:17461731 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM072822

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 8 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_Human1M-duo

About this variant

This variant overlaps 4 transcripts, has 264 individual genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variation displays