Original source

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

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

Chromosome 2:71602794 (forward strand) | View in location tab


with HGMD-PUBLIC CM980575 ; PhenCode DYSF:c.3892A>G (A/G)

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 27 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 17 transcripts, has 2504 individual genotypes and is associated with 5 phenotypes.

Variation displays