Variant (rsID / SNP)

rs10751478

rs10751478 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRRC2B. Location: chromosome 9, position 134,350,458. The table records no clinical significance for this variant.

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Reference-table entries

PRRC2BNot classified

Variant type: missense_variant
Chromosome / position: 9:134350458
HGVS: NM_001384818.1,c.2942C>T,p.Pro981Leu
Allele change: Missense_P981L

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.