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Variant (rsID / SNP)

rs3740861

ENDOD1

rs3740861 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ENDOD1. Location: chromosome 11, position 94,862,577. The table records no clinical significance for this variant.

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Reference-table entries

ENDOD1Not classified
Variant type
missense_variant
Chromosome / position
11:94862577
HGVS
NM_015036.3,c.1337G>T,p.Gly446Val
Allele change
Missense_G446V

Public references

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