Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs17271305
rs17271305
15 62040781 intron variant A/G;T snv
CUI: C0017741
Disease: Glucose tolerance test
Glucose tolerance test
0.800 1.000 1 2010 2010
dbSNP: rs369100678
rs369100678
0.925 0.040 15 61958608 missense variant C/G snv
PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET
0.800 1.000 1 2016 2016
dbSNP: rs148713408
rs148713408
15 61928573 intron variant C/T snv 8.7E-03
CUI: C0425782
Disease: Breast size
Breast size
0.700 1.000 1 2016 2016
dbSNP: rs17271340
rs17271340
15 62055686 intron variant C/T snv 0.33
CUI: C0017741
Disease: Glucose tolerance test
Glucose tolerance test
0.700 1.000 1 2018 2018
dbSNP: rs17271340
rs17271340
15 62055686 intron variant C/T snv 0.33
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement
0.700 1.000 1 2018 2018
dbSNP: rs2042608
rs2042608
15 61940181 intron variant C/A snv 0.48
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement
0.700 1.000 1 2018 2018
dbSNP: rs2042608
rs2042608
15 61940181 intron variant C/A snv 0.48
CUI: C0017741
Disease: Glucose tolerance test
Glucose tolerance test
0.700 1.000 1 2018 2018
dbSNP: rs369100678
rs369100678
0.925 0.040 15 61958608 missense variant C/G snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs72749754
rs72749754
15 62027233 intron variant G/A;C snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2017 2017
dbSNP: rs869312809
rs869312809
0.925 0.040 15 61915631 splice donor variant A/C snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs869312810
rs869312810
0.925 0.040 15 61882652 stop gained C/A snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs869312811
rs869312811
0.925 0.040 15 61947292 frameshift variant G/- delins
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs879253853
rs879253853
1.000 0.040 15 62013057 frameshift variant -/TCTG ins
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs933807
rs933807
15 61982741 intron variant G/A;C snv
CUI: C0424678
Disease: Lean body mass
Lean body mass
0.700 1.000 1 2019 2019
dbSNP: rs869312809
rs869312809
0.925 0.040 15 61915631 splice donor variant A/C snv
PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET
0.700 0
dbSNP: rs869312810
rs869312810
0.925 0.040 15 61882652 stop gained C/A snv
PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET
0.700 0
dbSNP: rs869312811
rs869312811
0.925 0.040 15 61947292 frameshift variant G/- delins
PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET
0.700 0
dbSNP: rs869320761
rs869320761
1.000 15 62013058 frameshift variant -/TCTG delins
PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET
0.700 0