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: rs11553746
rs11553746
ACP1
1.000 0.080 2 272203 missense variant C/T snv 0.31 0.28
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2017 2017
dbSNP: rs58461606
rs58461606
ACP1
2 267367 intron variant G/T snv 0.30
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs79716074
rs79716074
ACP1
2 277003 missense variant A/G snv 0.31 0.30
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs11553746
rs11553746
ACP1
1.000 0.080 2 272203 missense variant C/T snv 0.31 0.28
CUI: C0028754
Disease: Obesity
Obesity 		0.010 1.000 1 2018 2018
dbSNP: rs765467335
rs765467335
ACP1
1.000 0.160 2 277247 missense variant G/T snv 1.2E-05
CUI: C0175704
Disease: LEOPARD Syndrome
LEOPARD Syndrome 		0.010 1.000 1 2008 2008
dbSNP: rs774121564
rs774121564
ACP1
1.000 0.040 2 275197 missense variant C/G snv 4.1E-06
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		0.010 1.000 1 2013 2013