Variant (rsID / SNP)

rs1135173

rs1135173 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to INPP5D. Location: chromosome 2, position 234,054,873. The table records no clinical significance for this variant.

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Reference-table entries

INPP5DNot classified

Variant type: synonymous_variant
Chromosome / position: 2:234054873
HGVS: NM_001017915.3,c.738G>A,p.Ser246Ser
Allele change: Missense_R244H

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.