Source: ALL

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: rs111900181
rs111900181
1 54383167 intron variant A/G snv 9.1E-02
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement
0.700 1.000 1 2018 2018
dbSNP: rs150647904
rs150647904
1 54373812 intron variant -/CAG delins 9.8E-02
Platelet Component Distribution Width Measurement
0.700 1.000 1 2016 2016
dbSNP: rs3753414
rs3753414
1 54265482 intron variant C/G snv 0.42
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs3766432
rs3766432
1 54264279 intron variant G/C snv 5.3E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs562408
rs562408
1 54276945 intron variant A/G snv 0.61
CUI: C0429021
Disease: P wave duration (observable entity)
P wave duration (observable entity)
0.700 1.000 1 2017 2017
dbSNP: rs630602
rs630602
1 54263191 intron variant G/C snv 0.62
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2016 2016
dbSNP: rs630602
rs630602
1 54263191 intron variant G/C snv 0.62
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs643428
rs643428
1 54263185 intron variant C/G;T snv
CUI: C0337443
Disease: Sodium measurement
Sodium measurement
0.700 1.000 1 2019 2019
dbSNP: rs643428
rs643428
1 54263185 intron variant C/G;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2019 2019
dbSNP: rs80020578
rs80020578
1 54383154 intron variant G/A snv 9.0E-02
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement
0.700 1.000 1 2019 2019