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: rs12393627
rs12393627
ARSL
X 2967682 intron variant A/G snv 0.11
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2011 2012
dbSNP: rs12837147
rs12837147
ATP7A ; PGK1
X 77914078 intron variant C/T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs140498234
rs140498234 		X 106234538 intergenic variant T/C snv 1.6E-04
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs148300465
rs148300465 		X 130191451 intergenic variant T/C snv 2.4E-04
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs185781801
rs185781801
LOC105373146
X 21126732 intron variant T/C snv 4.6E-03
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs3848873
rs3848873 		X 119460459 downstream gene variant T/A;C snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs426349
rs426349 		X 140199935 intergenic variant C/T snv 0.44
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4844299
rs4844299 		X 71634424 regulatory region variant T/C snv 0.21
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs5938929
rs5938929 		X 77216412 intergenic variant G/C snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7058676
rs7058676
FAAH2
X 57322090 intron variant C/T snv 0.36
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7065171
rs7065171
LINC00629
X 134549560 upstream gene variant C/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs781838721
rs781838721
SHROOM4
X 50598688 intron variant A/G snv 1.6E-03
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs4821083
rs4821083
SYN3 ; LOC105373002
22 32660355 intron variant T/C snv 0.26
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2010 2019
dbSNP: rs1053593
rs1053593
HMGXB4
22 35264882 missense variant G/C;T snv 8.0E-06; 0.58
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1076301
rs1076301
SLC35E4
22 30648844 intron variant A/G snv 0.61
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10854521
rs10854521
MICAL3
22 17999834 intron variant G/A snv 0.20
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs114134839
rs114134839
SYN3 ; LOC105373002
22 32662616 intron variant G/A snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs11450220
rs11450220
PLA2G6 ; MAFF
22 38211527 intron variant -/G delins 0.58
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs118173451
rs118173451
TTC28-AS1
22 27960612 intron variant T/C snv 1.1E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs12170305
rs12170305
ZC3H7B
22 41346279 intron variant G/A snv 3.6E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs13057352
rs13057352
CERK
22 46699338 missense variant C/A snv 2.6E-02 2.6E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs134077
rs134077 		22 27667264 intergenic variant G/A snv 0.39
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs136029
rs136029
ATXN10
22 45840545 intron variant G/A snv 0.46
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs136139
rs136139
TBC1D22A
22 46992426 intron variant G/A;C snv 0.31
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs136872
rs136872
DEPDC5
22 31885582 intron variant A/G snv 0.94
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019