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Variant (rsID / SNP)

rs2289043

UNC5C

rs2289043 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UNC5C. Location: chromosome 4, position 96,106,322. The table records no clinical significance for this variant.

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Reference-table entries

UNC5CNot classified
Variant type
missense_variant
Chromosome / position
4:96106322
HGVS
NM_003728.4,c.2162T>C,p.Met721Thr
Allele change
Missense_M721T

Public references

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