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Variant (rsID / SNP)

rs17437781

GRB14

rs17437781 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRB14. Location: chromosome 2, position 165,424,837. The table records no clinical significance for this variant.

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Reference-table entries

GRB14Not classified
Variant type
synonymous_variant
Chromosome / position
2:165424837
HGVS
NM_001303422.2,c.51T>C,p.Ile17Ile
Allele change
Synonymous_I17I

Public references

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