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Variant (rsID / SNP)

rs2475298

SEC23IP

rs2475298 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SEC23IP. Location: chromosome 10, position 121,679,013. The table records no clinical significance for this variant.

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Reference-table entries

SEC23IPNot classified
Variant type
missense_variant
Chromosome / position
10:121679013
HGVS
NM_007190.4,c.1930A>G,p.Lys644Glu
Allele change
Missense_K644E

Public references

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