SERPINA5, serpin family A member 5, 5104

N. diseases: 185; N. variants: 11
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: rs10139745
rs10139745 		14 94569037 intron variant G/A snv 0.19
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs10146582
rs10146582 		14 94571441 intron variant G/A snv 0.19
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs10149354
rs10149354 		14 94572031 intron variant C/T snv 0.19
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs17091116
rs17091116 		14 94585537 intron variant C/G snv 0.30
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs5512
rs5512 		14 94568116 intron variant A/G snv 7.4E-03 7.3E-03
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs6119
rs6119 		14 94587675 missense variant A/G snv 0.14 0.23
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs6119
rs6119 		14 94587675 missense variant A/G snv 0.14 0.23
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2018 2018
dbSNP: rs8009930
rs8009930 		14 94582747 intron variant A/G;T snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1955656
rs1955656 		1.000 0.080 14 94579038 intron variant G/A snv 0.14
CUI: C0022660
Disease: Kidney Failure, Acute
Kidney Failure, Acute 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2093266
rs2093266 		1.000 0.080 14 94566450 intron variant G/A snv 0.15
CUI: C0022660
Disease: Kidney Failure, Acute
Kidney Failure, Acute 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2017 2017
dbSNP: rs6112
rs6112 		1.000 0.080 14 94587839 synonymous variant T/C snv 0.60 0.71
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma 		Neoplasms; Endocrine System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs6115
rs6115 		1.000 0.080 14 94587553 missense variant G/A;T snv 0.60
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma 		Neoplasms; Endocrine System Diseases 0.010 1.000 1 2013 2013