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: rs12127701
rs12127701
MYBPHL
1 109295642 intron variant A/G snv 6.2E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12127701
rs12127701
MYBPHL
1 109295642 intron variant A/G snv 6.2E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12127701
rs12127701
MYBPHL
1 109295642 intron variant A/G snv 6.2E-02
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		0.700 1.000 1 2018 2018
dbSNP: rs12127701
rs12127701
MYBPHL
1 109295642 intron variant A/G snv 6.2E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs17645031
rs17645031
MYBPHL
1 109292316 downstream gene variant C/T snv 7.9E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs17645031
rs17645031
MYBPHL
1 109292316 downstream gene variant C/T snv 7.9E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs17645031
rs17645031
MYBPHL
1 109292316 downstream gene variant C/T snv 7.9E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs407102
rs407102
MYBPHL
1 109303656 intron variant C/T snv 0.68
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs407102
rs407102
MYBPHL
1 109303656 intron variant C/T snv 0.68
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs41306199
rs41306199
MYBPHL
1 109292541 3 prime UTR variant C/T snv 7.8E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs41306199
rs41306199
MYBPHL
1 109292541 3 prime UTR variant C/T snv 7.8E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs41306199
rs41306199
MYBPHL
1 109292541 3 prime UTR variant C/T snv 7.8E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs413582
rs413582
MYBPHL
1 109308504 upstream gene variant C/T snv 0.37
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs413582
rs413582
MYBPHL
1 109308504 upstream gene variant C/T snv 0.37
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs413582
rs413582
MYBPHL
1 109308504 upstream gene variant C/T snv 0.37
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs600806
rs600806
MYBPHL
1 109298007 intron variant G/A;C snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs629001
rs629001
MYBPHL
1 109296296 missense variant C/G;T snv 0.93
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs629001
rs629001
MYBPHL
1 109296296 missense variant C/G;T snv 0.93
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs629001
rs629001
MYBPHL
1 109296296 missense variant C/G;T snv 0.93
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs638542
rs638542
MYBPHL
1 109302630 intron variant G/A snv 0.65
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs680434
rs680434
MYBPHL
1 109299649 intron variant C/T snv 0.65
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018