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Variant (rsID / SNP)

rs3750944

FHIP1B

rs3750944 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FHIP1B. Location: chromosome 11, position 6,239,344. The table records no clinical significance for this variant.

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Reference-table entries

FHIP1BNot classified
Variant type
missense_variant
Chromosome / position
11:6239344
HGVS
NM_032127.4,c.1514C>T,p.Thr505Met
Allele change
Missense_T491M

Public references

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