Variant (rsID / SNP)

rs62617790

rs62617790 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRAPPC11. Location: chromosome 4, position 184,618,936. Clinical significance in the table: Benign.

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Reference-table entries

TRAPPC11Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:184618936
Cytoband: 4q35.1
HGVS: NM_021942.6(TRAPPC11):c.2799G>C (p.Gln933His)
Allele change: Missense_Q933H

Associated conditions / phenotypes

Autosomal recessive limb-girdle muscular dystrophy type R18

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.