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Variant (rsID / SNP)

rs2278206

INPP4A

rs2278206 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to INPP4A. Location: chromosome 2, position 99,172,244. The table records no clinical significance for this variant.

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Reference-table entries

INPP4ANot classified
Variant type
missense_variant
Chromosome / position
2:99172244
HGVS
NM_001134224.2,c.1810A>G,p.Thr604Ala
Allele change
Silent

Public references

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