Variant (rsID / SNP)

rs61739385

rs61739385 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TUBGCP6. Location: chromosome 22, position 50,659,481. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

TUBGCP6Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 22:50659481
Cytoband: 22q13.33
HGVS: NM_020461.4(TUBGCP6):c.3307C>T (p.Arg1103Trp)
Allele change: Missense_R1103W

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.