INS, insulin, 3630

N. diseases: 405; N. variants: 37
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28933985
rs28933985
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C0342283
Disease:
Hyperproinsulinemia
G 0.840 CausalMutation CLINVAR
dbSNP: rs28933985
rs28933985
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C0342283
Disease:
Hyperproinsulinemia
T 0.840 CausalMutation CLINVAR
dbSNP: rs28933985
rs28933985
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C0342283
Disease:
Hyperproinsulinemia
A 0.840 CausalMutation CLINVAR
dbSNP: rs121918101
rs121918101
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C0342283
Disease:
Hyperproinsulinemia
C 0.810 CausalMutation CLINVAR
dbSNP: rs121908260
rs121908260
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C3150617
Disease:
Maturity-onset diabetes of the young, type 10
T 0.800 CausalMutation CLINVAR
dbSNP: rs121908261
rs121908261
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C1852092
Disease:
DIABETES MELLITUS, INSULIN-DEPENDENT, 2
A 0.800 CausalMutation CLINVAR
dbSNP: rs121908277
rs121908277
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C1833104
Disease:
DIABETES MELLITUS, PERMANENT NEONATAL
C 0.800 GeneticVariation CLINVAR
dbSNP: rs121908278
rs121908278
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C3150617
Disease:
Maturity-onset diabetes of the young, type 10
A 0.800 CausalMutation CLINVAR
dbSNP: rs80356663
rs80356663
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C1833104
Disease:
DIABETES MELLITUS, PERMANENT NEONATAL
T 0.800 CausalMutation CLINVAR
dbSNP: rs80356664
rs80356664
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C1833104
Disease:
DIABETES MELLITUS, PERMANENT NEONATAL
G 0.800 CausalMutation CLINVAR
dbSNP: rs80356664
rs80356664
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C1833104
Disease:
DIABETES MELLITUS, PERMANENT NEONATAL
T 0.800 CausalMutation CLINVAR
dbSNP: rs80356666
rs80356666
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C1833104
Disease:
DIABETES MELLITUS, PERMANENT NEONATAL
C 0.800 CausalMutation CLINVAR
dbSNP: rs80356667
rs80356667
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C1833104
Disease:
DIABETES MELLITUS, PERMANENT NEONATAL
A 0.800 CausalMutation CLINVAR
dbSNP: rs80356668
rs80356668
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C1833104
Disease:
DIABETES MELLITUS, PERMANENT NEONATAL
C 0.800 CausalMutation CLINVAR
dbSNP: rs80356669
rs80356669
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C1833104
Disease:
DIABETES MELLITUS, PERMANENT NEONATAL
A 0.800 CausalMutation CLINVAR
dbSNP: rs80356670
rs80356670
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C1833104
Disease:
DIABETES MELLITUS, PERMANENT NEONATAL
A 0.800 CausalMutation CLINVAR
dbSNP: rs80356671
rs80356671
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C1833104
Disease:
DIABETES MELLITUS, PERMANENT NEONATAL
T 0.800 CausalMutation CLINVAR
dbSNP: rs80356672
rs80356672
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C1833104
Disease:
DIABETES MELLITUS, PERMANENT NEONATAL
C 0.800 CausalMutation CLINVAR
dbSNP: rs121918102
rs121918102
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C0342283
Disease:
Hyperproinsulinemia
A 0.700 CausalMutation CLINVAR
dbSNP: rs148685531
rs148685531
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C0342283
Disease:
Hyperproinsulinemia
C 0.700 CausalMutation CLINVAR
dbSNP: rs1564912403
rs1564912403
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C1833104
Disease:
DIABETES MELLITUS, PERMANENT NEONATAL
C 0.700 GeneticVariation CLINVAR
dbSNP: rs397515519
rs397515519
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C1833104
Disease:
DIABETES MELLITUS, PERMANENT NEONATAL
C 0.700 CausalMutation CLINVAR
dbSNP: rs397515521
rs397515521
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C1833104
Disease:
DIABETES MELLITUS, PERMANENT NEONATAL
T 0.700 CausalMutation CLINVAR
dbSNP: rs397515521
rs397515521
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C1833104
Disease:
DIABETES MELLITUS, PERMANENT NEONATAL
A 0.700 CausalMutation CLINVAR
dbSNP: rs797045623
rs797045623
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C1833104
Disease:
DIABETES MELLITUS, PERMANENT NEONATAL
T 0.700 CausalMutation CLINVAR