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Variant (rsID / SNP)

rs130079

CCHCR1

rs130079 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCHCR1. Location: chromosome 6, position 31,112,737. The table records no clinical significance for this variant.

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Reference-table entries

CCHCR1Not classified
Variant type
missense_variant
Chromosome / position
6:31112737
HGVS
NM_001394641.1,c.2017G>T,p.Gly673Cys
Allele change
Missense_G628C

Public references

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