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Variant (rsID / SNP)

rs130075

CCHCR1

rs130075 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCHCR1. Location: chromosome 6, position 31,122,502. The table records no clinical significance for this variant.

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Reference-table entries

CCHCR1Not classified
Variant type
missense_variant
Chromosome / position
6:31122502
HGVS
NM_001394641.1,c.599G>A,p.Arg200Gln
Allele change
Missense_R155Q

Public references

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