Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0023980
Disease: Longevity
Longevity
0.700 1.000 2 2016 2019
dbSNP: rs2075650
rs2075650
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C0023980
Disease: Longevity
Longevity
0.800 1.000 2 2011 2012
dbSNP: rs10256972
rs10256972
7 999367 intron variant A/C snv 0.62
CUI: C0023980
Disease: Longevity
Longevity
0.800 1.000 1 2010 2010
dbSNP: rs10445407
rs10445407
17 81288009 intron variant C/A;T snv
CUI: C0023980
Disease: Longevity
Longevity
0.800 1.000 1 2010 2010
dbSNP: rs10957550
rs10957550
8 71382353 intron variant G/A;C snv
CUI: C0023980
Disease: Longevity
Longevity
0.700 1.000 1 2014 2014
dbSNP: rs1262476
rs1262476
6 126665850 intron variant A/G;T snv
CUI: C0023980
Disease: Longevity
Longevity
0.700 1.000 1 2019 2019
dbSNP: rs13008689
rs13008689
2 8390126 intron variant G/A snv 0.35
CUI: C0023980
Disease: Longevity
Longevity
0.800 1.000 1 2010 2010
dbSNP: rs13118159
rs13118159
4 1371339 intron variant T/C snv 0.55
CUI: C0023980
Disease: Longevity
Longevity
0.800 1.000 1 2010 2010
dbSNP: rs1327533
rs1327533
9 110368883 intron variant T/G snv 8.7E-02
CUI: C0023980
Disease: Longevity
Longevity
0.800 1.000 1 2010 2010
dbSNP: rs1356888
rs1356888
2 50288880 intron variant T/A;C snv
CUI: C0023980
Disease: Longevity
Longevity
0.800 1.000 1 2010 2010
dbSNP: rs16975963
rs16975963
19 37834896 intron variant C/G snv 0.25
CUI: C0023980
Disease: Longevity
Longevity
0.800 1.000 1 2010 2010
dbSNP: rs2024714
rs2024714
20 61637438 intron variant C/T snv 0.60
CUI: C0023980
Disease: Longevity
Longevity
0.800 1.000 1 2010 2010
dbSNP: rs2149954
rs2149954
0.882 0.080 5 158393594 intron variant C/T snv 0.37
CUI: C0023980
Disease: Longevity
Longevity
0.700 1.000 1 2014 2014
dbSNP: rs2273
rs2273
4 75968235 intron variant C/T snv 0.33
CUI: C0023980
Disease: Longevity
Longevity
0.800 1.000 1 2010 2010
dbSNP: rs2440012
rs2440012
13 18865983 intron variant C/A;G snv
CUI: C0023980
Disease: Longevity
Longevity
0.700 1.000 1 2016 2016
dbSNP: rs2704588
rs2704588
4 88928621 intron variant T/C snv 0.19
CUI: C0023980
Disease: Longevity
Longevity
0.700 1.000 1 2016 2016
dbSNP: rs2758603
rs2758603
1 156229203 intron variant T/C snv 0.37
CUI: C0023980
Disease: Longevity
Longevity
0.700 1.000 1 2019 2019
dbSNP: rs2826891
rs2826891
21 21537795 intron variant C/T snv 0.43 0.47
CUI: C0023980
Disease: Longevity
Longevity
0.800 1.000 1 2010 2010
dbSNP: rs3106598
rs3106598
13 61104778 intron variant G/A snv 0.43
CUI: C0023980
Disease: Longevity
Longevity
0.800 1.000 1 2010 2010
dbSNP: rs3212335
rs3212335
1.000 0.080 15 26766994 intron variant C/T snv 0.32
CUI: C0023980
Disease: Longevity
Longevity
0.800 1.000 1 2010 2010
dbSNP: rs35262860
rs35262860
RP1
8 54566349 intron variant -/CT delins 0.31
CUI: C0023980
Disease: Longevity
Longevity
0.700 1.000 1 2019 2019
dbSNP: rs3847687
rs3847687
12 131040508 intron variant C/A;T snv 0.35
CUI: C0023980
Disease: Longevity
Longevity
0.800 1.000 1 2010 2010
dbSNP: rs4148546
rs4148546
13 95028031 intron variant G/A snv 0.55
CUI: C0023980
Disease: Longevity
Longevity
0.800 1.000 1 2010 2010
dbSNP: rs432203
rs432203
2 70537556 intron variant C/A snv 0.58
CUI: C0023980
Disease: Longevity
Longevity
0.800 1.000 1 2010 2010
dbSNP: rs4468878
rs4468878
20 61353181 intron variant T/C snv 0.51
CUI: C0023980
Disease: Longevity
Longevity
0.800 1.000 1 2010 2010