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: rs10136766
rs10136766
IGHG3 ; LOC105378184
14 105766248 intron variant A/G snv 0.49
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs11628528
rs11628528
IGHG3
14 105770121 synonymous variant C/T snv 0.48; 5.2E-06 0.48
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs150015846
rs150015846
IGHG3
14 105768960 intron variant C/A;T snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs77307099
rs77307099
IGHG3
14 105769430 missense variant C/T snv 4.3E-05; 0.34 0.26
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018