Variant (rsID / SNP)
rs2903250
rs2903250 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IGSF11. Location: chromosome 3, position 118,649,060. The table records no clinical significance for this variant.
Reference-table entries
IGSF11Not classified
- Variant type
- missense_variant
- Chromosome / position
- 3:118649060
- HGVS
- NM_001353318.2,c.265C>A,p.Pro89Thr
- Allele change
- Missense_P39T
Associated conditions / phenotypes
Missense_P39T|Silent|Missense_P39T|Missense_P89T|Missense_P38T|Missense_P38T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.