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: rs7398357
rs7398357
ANKS1B
12 99493896 intron variant G/A snv 0.16
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs2175523
rs2175523
ANKS1B
12 99489754 intron variant G/C snv 0.15
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs7579999
rs7579999 		2 99241207 intron variant G/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs10865030
rs10865030
MRPL30
2 99188179 splice region variant T/C;G snv 0.87 0.83
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs4851189
rs4851189
LIPT1 ; TSGA10
2 99153581 intron variant T/C snv 0.83
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs17028615
rs17028615
ADH4 ; LOC100507053
1.000 0.080 4 99150767 intron variant A/C;G snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2014 2014
dbSNP: rs4850896
rs4850896
TSGA10
2 99137979 intron variant G/A;C;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs12712034
rs12712034
KIAA1211L
2 98842470 intron variant G/A;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs10883094
rs10883094
HPS1
10 98428349 intron variant G/A snv 0.27
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs7921146
rs7921146
HPS1
10 98426844 intron variant G/A snv 0.37
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs2296434
rs2296434
HPS1
10 98423813 missense variant G/C;T snv 0.11; 4.8E-05
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs2296435
rs2296435
HPS1
10 98422528 intron variant T/C snv 0.27 0.22
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs17109834
rs17109834
HPS1
10 98422090 intron variant T/C snv 0.17
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs2296436
rs2296436
HPS1
10 98420094 missense variant T/A;C snv 1.0E-01
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs11189600
rs11189600
HPS1
1.000 0.040 10 98419517 intron variant C/A;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs701801
rs701801
HPS1 ; PYROXD2
1.000 0.040 10 98417112 3 prime UTR variant C/T snv 0.39
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs3830019
rs3830019
HPS1 ; PYROXD2
10 98417091 3 prime UTR variant C/A;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs3830020
rs3830020
HPS1 ; PYROXD2
10 98416858 3 prime UTR variant G/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs1739
rs1739
HPS1 ; PYROXD2
10 98416582 3 prime UTR variant A/G snv 0.46
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs1061437
rs1061437
HPS1 ; PYROXD2
10 98416397 3 prime UTR variant C/T snv 0.35
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs3750605
rs3750605
HPS1 ; PYROXD2
10 98415897 upstream gene variant C/T snv 0.27
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs3750604
rs3750604
HPS1 ; PYROXD2
10 98415824 upstream gene variant G/A snv 0.21
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs8181292
rs8181292
HPS1 ; PYROXD2
10 98415720 upstream gene variant A/G snv 0.38
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs2274244
rs2274244
PYROXD2
10 98415461 upstream gene variant A/G snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs2147900
rs2147900
PYROXD2
10 98414964 intron variant T/C snv 0.34 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013