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Variant (rsID / SNP)

rs2640785

EXPH5

rs2640785 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EXPH5. Location: chromosome 11, position 108,409,784. The table records no clinical significance for this variant.

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Reference-table entries

EXPH5Not classified
Variant type
missense_variant
Chromosome / position
11:108409784
HGVS
NM_015065.3,c.410A>T,p.Glu137Val
Allele change
Missense_E61V

Public references

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