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Variant (rsID / SNP)

rs7645033

PARP14

rs7645033 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PARP14. Location: chromosome 3, position 122,437,321. The table records no clinical significance for this variant.

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Reference-table entries

PARP14Not classified
Variant type
synonymous_variant
Chromosome / position
3:122437321
HGVS
NM_017554.3,c.4323T>C,p.Tyr1441Tyr
Allele change
Synonymous_Y1441Y

Public references

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