Original source

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

Alleles
C/G/T | Ancestral: C | Ambiguity code: B
Location

Chromosome 11:34966740 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM042447

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 1 individual genotype and is associated with 1 phenotype.

Variation displays