Gene: ALDH1A2 ×
Source: GWASCAT ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1800588
rs1800588
LIPC ; ALDH1A2
3 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.800 1.000 5 2012 2019
dbSNP: rs1532085
rs1532085
ALDH1A2
7 0.882 0.080 15 58391167 intron variant A/G;T snv 0.800 1.000 4 2010 2019
dbSNP: rs261342
rs261342
LIPC ; ALDH1A2 ; LIPC-AS1
3 15 58438954 intron variant G/A;C;T snv 0.800 1.000 2 2012 2019
dbSNP: rs4775041
rs4775041
ALDH1A2
4 1.000 0.040 15 58382496 intron variant G/C snv 0.24 0.800 1.000 2 2008 2018
dbSNP: rs10468017
rs10468017
ALDH1A2
6 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.800 1.000 1 2009 2018
dbSNP: rs261332
rs261332
LIPC ; ALDH1A2 ; LIPC-AS1
17 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 0.800 1.000 1 2012 2016
dbSNP: rs588136
rs588136
LIPC ; ALDH1A2 ; LIPC-AS1
2 15 58438299 intron variant C/G;T snv 0.800 1.000 1 2012 2017
dbSNP: rs1077835
rs1077835
LIPC ; ALDH1A2
3 15 58431227 intron variant A/G snv 0.34 0.700 1.000 5 2015 2019
dbSNP: rs1077834
rs1077834
LIPC ; ALDH1A2
4 15 58431280 intron variant T/C snv 0.34 0.700 1.000 2 2018 2019
dbSNP: rs261291
rs261291
ALDH1A2
4 1.000 0.080 15 58387979 intron variant T/A;C snv 0.700 1.000 2 2018 2018
dbSNP: rs7350789
rs7350789
ALDH1A2
3 15 58387469 intron variant G/A snv 0.35 0.700 1.000 2 2018 2019
dbSNP: rs13329672
rs13329672
ALDH1A2
3 15 58407738 intron variant C/T snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs1601935
rs1601935
ALDH1A2
3 15 58379566 intron variant G/T snv 0.60 0.700 1.000 1 2018 2018
dbSNP: rs2043082
rs2043082
ALDH1A2
4 15 58382109 intron variant G/A snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs261334
rs261334
LIPC ; ALDH1A2 ; LIPC-AS1
3 15 58434545 intron variant G/C snv 0.73 0.700 1.000 1 2018 2018