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Variant (rsID / SNP)

rs2278211

INPP4A

rs2278211 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to INPP4A. Location: chromosome 2, position 99,149,946. The table records no clinical significance for this variant.

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Reference-table entries

INPP4ANot classified
Variant type
synonymous_variant
Chromosome / position
2:99149946
HGVS
NM_001134224.2,c.258G>A,p.Thr86Thr
Allele change
Synonymous_T86T

Associated conditions / phenotypes

Synonymous_T86T|Synonymous_T86T|Synonymous_T86T|Synonymous_T86T|Synonymous_T86T

Public references

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