Original source

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

Alleles
G/C/T | Ancestral: G | Ambiguity code: B | MAF: < 0.01 (C)
Location

Chromosome 17:43115792 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

Synonyms

LSDB U14680.1:c.81-13C>G, U14680.1:c.81-13C>A

This variant has 48 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 44 transcripts, has 2504 sample genotypes and is associated with 5 phenotypes.

Variant displays