ClinVar Miner

List of variants in gene combination INS, INS-IGF2 reported as uncertain significance by Clinical Genomics, Uppaluri K&H Personalized Medicine Clinic

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000207.3(INS):c.63A>G (p.Pro21=) rs11564720 0.00546
NM_000207.3(INS):c.147C>T (p.Phe49=) rs148685531 0.00016
NM_000207.3(INS):c.130G>A (p.Gly44Arg) rs765512575 0.00003
NM_000207.3(INS):c.202C>A (p.Leu68Met) rs121908279 0.00002
NM_000207.3(INS):c.266G>A (p.Arg89His) rs28933985 0.00002
NM_000207.3(INS):c.25C>T (p.Pro9Ser) rs372122432 0.00001
NM_000207.3(INS):c.-18+62C>T rs1166335966
NM_000207.3(INS):c.100C>G (p.His34Asp) rs121918101
NM_000207.3(INS):c.125T>C (p.Val42Ala) rs886037863
NM_000207.3(INS):c.137G>A (p.Arg46Gln) rs121908260
NM_000207.3(INS):c.140G>T (p.Gly47Val) rs80356667
NM_000207.3(INS):c.187+241G>A rs886041083
NM_000207.3(INS):c.250G>A (p.Gly84Arg) rs121908274
NM_000207.3(INS):c.265C>T (p.Arg89Cys) rs80356669
NM_000207.3(INS):c.268G>T (p.Gly90Cys) rs80356670
NM_000207.3(INS):c.274G>T (p.Val92Leu) rs121918102
NM_000207.3(INS):c.287G>A (p.Cys96Tyr) rs80356671
NM_000207.3(INS):c.3G>A (p.Met1Ile) rs397515521
NM_000207.3(INS):c.67G>A (p.Ala23Thr) rs13306444
NM_000207.3(INS):c.85C>G (p.His29Asp) rs121908272
NM_000207.3(INS):c.94G>A (p.Gly32Ser) rs80356664

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.