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Variant (rsID / SNP)

rs10420258

GPATCH1

rs10420258 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPATCH1. Location: chromosome 19, position 33,602,757. The table records no clinical significance for this variant.

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Reference-table entries

GPATCH1Not classified
Variant type
synonymous_variant
Chromosome / position
19:33602757
HGVS
NM_018025.3,c.1713C>T,p.His571His
Allele change
Synonymous_H571H

Public references

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