Variant: rs121964995

present in Gene: INVS present in Chromosome: 9 Position on Chromosome: 100264835 Alleles of this Variant: T/C

rs121964995 in INVS gene and NEPHRONOPHTHISIS 2 PMID 12872123 2003 Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination.