Variant (rsID / SNP)
rs3824658
rs3824658 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ITIH5. Location: chromosome 10, position 7,605,067. The table records no clinical significance for this variant.
Reference-table entries
ITIH5Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:7605067
- HGVS
- NM_030569.7,c.2807G>A,p.Arg936Gln
- Allele change
- Missense_R722Q
Associated conditions / phenotypes
Rectum Cancer|Type 2 Diabetes Mellitus|Diabetes Mellitus
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.