Variant (rsID / SNP)

rs34536443

rs34536443 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TYK2. Location: chromosome 19, position 10,463,118. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

TYK2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 19:10463118
Cytoband: 19p13.2
HGVS: NM_003331.5(TYK2):c.3310C>G (p.Pro1104Ala)
Allele change: Missense_P1104A

Associated conditions / phenotypes

Immunodeficiency 35

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.