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Variant (rsID / SNP)

rs17647806

ITPRID2

rs17647806 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ITPRID2. Location: chromosome 2, position 182,780,874. The table records no clinical significance for this variant.

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Reference-table entries

ITPRID2Not classified
Variant type
missense_variant
Chromosome / position
2:182780874
HGVS
NM_001130445.3,c.2507C>T,p.Pro836Leu
Allele change
Missense_P836L

Public references

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