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Variant (rsID / SNP)

rs836237

SP100

rs836237 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SP100. Location: chromosome 2, position 231,406,680. The table records no clinical significance for this variant.

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Reference-table entries

SP100Not classified
Variant type
missense_variant
Chromosome / position
2:231406680
HGVS
NM_001080391.2,c.2477T>C,p.Met826Thr
Allele change
Missense_M826T

Public references

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