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Variant (rsID / SNP)

rs4973588

NGEF

rs4973588 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NGEF. Location: chromosome 2, position 233,834,975. The table records no clinical significance for this variant.

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Reference-table entries

NGEFNot classified
Variant type
missense_variant
Chromosome / position
2:233834975
HGVS
NM_019850.3,c.332T>C,p.Met111Thr
Allele change
Missense_M111T

Public references

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