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: rs11165867
rs11165867
1 1.000 0.040 1 97412512 intron variant C/T snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs36025579
rs36025579
1 1.000 0.040 1 97337068 intron variant A/G snv 0.26 0.700 1.000 1 2017 2017
dbSNP: rs4271249
rs4271249
1 1.000 0.040 1 97933063 intron variant G/T snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs61789073
rs61789073
2 1.000 0.040 1 97938540 intron variant T/C snv 4.9E-02 0.700 1.000 1 2017 2017
dbSNP: rs6685859
rs6685859
2 1.000 0.040 1 97357213 intron variant G/C snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs76869799
rs76869799
1 1.000 0.040 1 97368969 intron variant C/G snv 2.6E-02 0.700 1.000 1 2015 2015
dbSNP: rs80289781
rs80289781
2 1.000 0.040 1 97980274 intron variant C/G;T snv 0.700 1.000 1 2019 2019