Variant (rsID / SNP)

rs35155575

rs35155575 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PAX4. Location: chromosome 7, position 127,255,466. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

PAX4Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 7:127255466
Cytoband: 7q32.1
HGVS: NM_001366110.1(PAX4):c.133C>T (p.Arg45Trp)
Allele change: Missense_R37W

Associated conditions / phenotypes

Diabetes mellitus, ketosis-prone, susceptibility to

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.