Variant (rsID / SNP)

rs3745600

rs3745600 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PPAN-P2RY11, P2RY11. Location: chromosome 19, position 10,224,526. The table records no clinical significance for this variant.

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Reference-table entries

PPAN-P2RY11Not classified

Variant type: missense_variant
Chromosome / position: 19:10224526
HGVS: NM_001198690.2,c.1559C>T,p.Pro520Leu
Allele change: Synonymous_A499A

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.