Variant (rsID / SNP)

rs61729681

rs61729681 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PARP12. Location: chromosome 7, position 139,757,712. The table records no clinical significance for this variant.

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Reference-table entries

PARP12Not classified

Variant type: missense_variant
Chromosome / position: 7:139757712
HGVS: NM_022750.4,c.449G>T,p.Trp150Leu
Allele change: Missense_W150L

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.