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: rs13394619
rs13394619
1.000 0.040 2 11587381 splice acceptor variant G/A snv 0.53 0.61
CUI: C0014175
Disease: Endometriosis
Endometriosis
Female Urogenital Diseases and Pregnancy Complications 0.840 1.000 4 2012 2015
dbSNP: rs11674184
rs11674184
1.000 0.040 2 11581409 intron variant T/A;G snv
CUI: C0014175
Disease: Endometriosis
Endometriosis
Female Urogenital Diseases and Pregnancy Complications 0.710 0.500 2 2017 2019
dbSNP: rs10929757
rs10929757
1.000 2 11562535 missense variant A/C snv 0.54 0.44
CUI: C2242776
Disease: Plexiform leiomyoma
Plexiform leiomyoma
0.700 1.000 1 2018 2018
dbSNP: rs10929757
rs10929757
1.000 2 11562535 missense variant A/C snv 0.54 0.44
CUI: C0042133
Disease: Uterine Fibroids
Uterine Fibroids
Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs113467400
rs113467400
2 11580173 intron variant C/T snv 0.11
CUI: C1314691
Disease: Age at menarche
Age at menarche
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs1435547
rs1435547
1.000 0.080 2 11597965 missense variant T/A;C snv 0.98
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs148143917
rs148143917
1.000 2 11524625 intron variant A/C snv 9.8E-03
CUI: C2242776
Disease: Plexiform leiomyoma
Plexiform leiomyoma
0.700 1.000 1 2018 2018
dbSNP: rs148143917
rs148143917
1.000 2 11524625 intron variant A/C snv 9.8E-03
CUI: C0042133
Disease: Uterine Fibroids
Uterine Fibroids
Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs149940960
rs149940960
1.000 0.120 2 11641492 3 prime UTR variant T/C snv 1.0E-02
Serum Alanine Aminotransferase Measurement
0.700 1.000 1 2017 2017
dbSNP: rs149940960
rs149940960
1.000 0.120 2 11641492 3 prime UTR variant T/C snv 1.0E-02
Precursor Cell Lymphoblastic Leukemia Lymphoma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2017 2017
dbSNP: rs149940960
rs149940960
1.000 0.120 2 11641492 3 prime UTR variant T/C snv 1.0E-02
Alanine aminotransferase measurement
0.700 1.000 1 2017 2017
dbSNP: rs16857586
rs16857586
2 11532217 intron variant C/A;T snv
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs35417544
rs35417544
1.000 2 11540277 intron variant C/T snv 0.59
CUI: C2242776
Disease: Plexiform leiomyoma
Plexiform leiomyoma
0.700 1.000 1 2019 2019
dbSNP: rs35417544
rs35417544
1.000 2 11540277 intron variant C/T snv 0.59
CUI: C0042133
Disease: Uterine Fibroids
Uterine Fibroids
Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs73175262
rs73175262
2 11618305 missense variant G/A snv 2.4E-03 9.9E-03
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012
dbSNP: rs77294520
rs77294520
1.000 0.040 2 11520829 intron variant G/A;C;T snv
CUI: C0014175
Disease: Endometriosis
Endometriosis
Female Urogenital Diseases and Pregnancy Complications 0.700 1.000 1 2017 2017