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Variant (rsID / SNP)

rs130076

CCHCR1

rs130076 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCHCR1. Location: chromosome 6, position 31,122,482. The table records no clinical significance for this variant.

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Reference-table entries

CCHCR1Not classified
Variant type
missense_variant
Chromosome / position
6:31122482
HGVS
NM_001394641.1,c.619C>T,p.Arg207Trp
Allele change
Missense_R162W

Associated conditions / phenotypes

Pustulosis of Palm and Sole|Psoriasis

Public references

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