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Variant (rsID / SNP)

rs3732031

NOSTRIN

rs3732031 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NOSTRIN. Location: chromosome 2, position 169,681,151. The table records no clinical significance for this variant.

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Reference-table entries

NOSTRINNot classified
Variant type
synonymous_variant
Chromosome / position
2:169681151
HGVS
NM_001171631.2,c.121C>T,p.Leu41Leu
Allele change
Synonymous_L41L

Public references

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