Variant (rsID / SNP)

rs10410258

rs10410258 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GIPC3. Location: chromosome 19, position 3,592,730. The table records no clinical significance for this variant.

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Reference-table entries

GIPC3Not classified

Variant type: 3_prime_UTR_variant
Chromosome / position: 19:3592730
HGVS: NM_133261.3,c.*2542C>T
Allele change: Silent

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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