Variant (rsID / SNP)

rs2275069

rs2275069 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ITIH5. Location: chromosome 10, position 7,618,686. The table records no clinical significance for this variant.

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Reference-table entries

ITIH5Not classified

Variant type: missense_variant
Chromosome / position: 10:7618686
HGVS: NM_030569.7,c.1708A>C,p.Thr570Pro
Allele change: Missense_T356P

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.