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Variant (rsID / SNP)

rs74785222

CLHC1

rs74785222 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLHC1. Location: chromosome 2, position 55,449,412. The table records no clinical significance for this variant.

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Reference-table entries

CLHC1Not classified
Variant type
missense_variant
Chromosome / position
2:55449412
HGVS
NM_152385.4,c.136G>T,p.Ala46Ser
Allele change
Missense_A46S

Public references

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