Variant (rsID / SNP)

rs78681604

rs78681604 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TJP2. Location: chromosome 9, position 71,840,944. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

TJP2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 9:71840944
Cytoband: 9q21.11
HGVS: NM_004817.4(TJP2):c.1063G>C (p.Gly355Arg)
Allele change: Missense_G332R

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.