Source: GWASCAT

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: rs7977418
rs7977418
CCDC91
12 28435309 intron variant T/C snv 0.40
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 2 2019 2019
dbSNP: rs803765
rs803765
LINC00348
13 71073456 intron variant C/A;T snv
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 2 2019 2019
dbSNP: rs8069451
rs8069451
FBXL20
17 39348680 intron variant T/C snv 0.39
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 2 2019 2019
dbSNP: rs9788269
rs9788269
CRADD
12 93801114 intron variant A/G snv 0.23
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 2 2019 2019
dbSNP: rs10067798
rs10067798
TENM2
5 167413686 intron variant T/A snv 0.44
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs1008833
rs1008833
PIK3C2B
1 204457167 intron variant A/G snv 0.12
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs10128597
rs10128597
TRIM66
11 8673283 intron variant G/A snv 0.27
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs1013105
rs1013105
SHROOM3
4 76687512 intron variant G/A;T snv
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs10168801
rs10168801
DIRC3
2 217715827 intron variant G/A snv 0.66
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs10172309
rs10172309
CCNYL1
2 207743915 intron variant G/C snv 2.7E-02
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs10184849
rs10184849
PCBP1-AS1
2 70034525 intron variant T/A;C snv
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs10201883
rs10201883 		2 177606679 intron variant T/C snv 0.82
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs10209172
rs10209172
MFSD6 ; NEMP2
2 190504195 intron variant G/A;C snv
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs1035101
rs1035101 		2 59563217 intron variant C/T snv 0.60
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs10410606
rs10410606
LTBP4
19 40603069 intron variant A/C snv 0.52
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs1041733
rs1041733 		21 34311960 intron variant T/A snv 0.49
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs10737680
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs10779158
rs10779158
LINC02820
12 85330318 intron variant A/G;T snv 0.49
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2018 2018
dbSNP: rs10787268
rs10787268
RBM20
10 110685953 intron variant C/T snv 0.30
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs1079572
rs1079572
WWOX
16 78153241 intron variant G/A snv 0.57
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2014 2014
dbSNP: rs10838435
rs10838435
PRDM11
11 45223352 intron variant C/G snv 0.70
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs10848835
rs10848835
TSPAN9
12 3232344 intron variant G/C snv 8.4E-02
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs10852506
rs10852506
PKD1L3
16 71936042 intron variant T/C snv 0.38
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs10853628
rs10853628
DCC
18 53244268 intron variant T/C snv 0.42
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs10858246
rs10858246
QSOX2
9 136210985 intron variant G/C snv 0.23
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2017 2017