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: rs67585357
rs67585357
RTL1 ; MIR433 ; MIR431
14 100879977 3 prime UTR variant C/T snv 0.16
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs2181834
rs2181834 		10 100901494 intergenic variant G/T snv 0.45
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs13244629
rs13244629 		7 100911633 intergenic variant A/C snv 0.14
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs11247252
rs11247252
LRRK1
15 101018722 intron variant G/A snv 0.42
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs8922
rs8922
NALCN ; NALCN-AS1
13 101053841 3 prime UTR variant A/C snv 0.17
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7026834
rs7026834
PLPPR1
9 101129097 intron variant C/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs3020623
rs3020623
SERPINE1
7 101129564 intron variant G/A snv 0.32
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4965800
rs4965800 		15 101162696 regulatory region variant A/C;G snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs62621400
rs62621400
CHSY1
15 101178034 missense variant C/G snv 6.2E-02 4.4E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs117246624
rs117246624
TMEM259
19 1012003 intron variant A/G snv 0.15 0.14
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs72768580
rs72768580
CHSY1
15 101234403 intron variant A/G snv 0.12
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7795865
rs7795865
AZGP1P2
7 101289303 intron variant C/T snv 9.6E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4323860
rs4323860
SBF2
11 10138336 intron variant T/C snv 0.50
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs2320549
rs2320549
GAS7
17 10141230 intron variant A/G;T snv 0.32
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs78333947
rs78333947
DNMT1
19 10143085 intron variant G/A snv 3.6E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs933089
rs933089 		13 101447688 upstream gene variant A/G snv 0.32
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs11247294
rs11247294
PCSK6
15 101467412 intron variant C/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs12905213
rs12905213
PCSK6
15 101475115 intron variant C/G snv 0.75
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs13062095
rs13062095 		3 101548541 intergenic variant T/C snv 0.24
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs34587452
rs34587452
FGFRL1
4 1016112 intron variant G/C snv 0.14
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1955614
rs1955614 		14 101624585 downstream gene variant T/C snv 0.13
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs78229644
rs78229644 		3 101638262 regulatory region variant T/G snv 5.8E-03
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs10883674
rs10883674
FBXW4
10 101665811 intron variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs116967872
rs116967872 		7 101712043 intergenic variant A/G snv 2.7E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs6650791
rs6650791
MAP4K4
2 101741872 intron variant C/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019