Variant (rsID / SNP)

rs34774441

rs34774441 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TJP2. Location: chromosome 9, position 71,851,877. Clinical significance in the table: Benign.

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Reference-table entries

TJP2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 9:71851877
Cytoband: 9q21.11
HGVS: NM_004817.4(TJP2):c.2004G>A (p.Met668Ile)
Allele change: Missense_M645I

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.