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Variant (rsID / SNP)

rs1046756

PRRC2A

rs1046756 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRRC2A. Location: chromosome 6, position 31,605,278. The table records no clinical significance for this variant.

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Reference-table entries

PRRC2ANot classified
Variant type
missense_variant
Chromosome / position
6:31605278
HGVS
NM_004638.4,c.6389C>T,p.Pro2130Leu
Allele change
Missense_P2130L

Public references

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