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Variant (rsID / SNP)

rs10200024

CROCC2

rs10200024 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CROCC2. Location: chromosome 2, position 241,929,228. The table records no clinical significance for this variant.

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Reference-table entries

CROCC2Not classified
Variant type
missense_variant
Chromosome / position
2:241929228
HGVS
NM_001351305.2,c.4841A>G,p.Gln1614Arg
Allele change
Missense_Q1614R

Public references

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