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Variant (rsID / SNP)

rs1134766

PATJ

rs1134766 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PATJ. Location: chromosome 1, position 62,380,270. The table records no clinical significance for this variant.

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Reference-table entries

PATJNot classified
Variant type
synonymous_variant
Chromosome / position
1:62380270
HGVS
NM_001350145.3,c.3504C>T,p.Asn1168Asn
Allele change
Synonymous_N1168N

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.