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Variant (rsID / SNP)

rs10770125

INS-IGF2IGF2

rs10770125 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to INS-IGF2, IGF2. Location: chromosome 11, position 2,169,014. The table records no clinical significance for this variant.

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Reference-table entries

INS-IGF2Not classified
Variant type
missense_variant
Chromosome / position
11:2169014
HGVS
NM_001042376.3,c.431T>C,p.Leu144Pro
Allele change
Silent

Associated conditions / phenotypes

Gestational Diabetes|Microvascular Complications of Diabetes 6|Microvascular Complications of Diabetes 4|Microvascular Complications of Diabetes 3|Microvascular Complications of Diabetes 7

Public references

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