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: rs121913628
rs121913628
10 0.763 0.160 14 23424059 missense variant C/G;T snv 0.700 0
dbSNP: rs141735183
rs141735183
1 14 23420222 stop gained C/A snv 8.2E-06 7.0E-06 0.700 0
dbSNP: rs148808089
rs148808089
4 0.882 0.080 14 23429038 missense variant G/A snv 2.0E-05 1.4E-05 0.700 0
dbSNP: rs3218713
rs3218713
10 0.763 0.160 14 23431468 missense variant C/A;T snv 0.700 0
dbSNP: rs397516088
rs397516088
4 0.882 0.080 14 23429850 missense variant C/G;T snv 0.700 0
dbSNP: rs397516142
rs397516142
3 1.000 0.080 14 23425357 missense variant C/A;G;T snv 8.0E-06; 1.6E-05 0.700 0
dbSNP: rs397516165
rs397516165
4 0.925 0.080 14 23424118 missense variant C/G;T snv 0.700 0
dbSNP: rs397516260
rs397516260
4 0.882 0.080 14 23431789 missense variant C/A;T snv 1.6E-05 0.700 0
dbSNP: rs397516269
rs397516269
4 0.882 0.080 14 23431426 missense variant A/G snv 4.0E-06 0.700 0
dbSNP: rs45516091
rs45516091
2 14 23431608 missense variant G/A snv 1.2E-05 7.0E-06 0.700 0
dbSNP: rs45544633
rs45544633
4 1.000 0.080 14 23417174 missense variant G/A snv 0.700 0
dbSNP: rs727503246
rs727503246
4 0.882 0.080 14 23418313 missense variant C/T snv 7.0E-06 0.700 0
dbSNP: rs730880895
rs730880895
1 14 23425373 missense variant C/T snv 0.700 0
dbSNP: rs730880903
rs730880903
1 14 23422268 missense variant G/A snv 0.700 0
dbSNP: rs1343372308
rs1343372308
2 14 23413792 missense variant C/G snv 7.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs371855540
rs371855540
2 14 23415095 missense variant C/T snv 2.0E-05 3.5E-05 0.010 1.000 1 2016 2016
dbSNP: rs727503249
rs727503249
2 1.000 0.040 14 23419588 missense variant G/A;C snv 0.010 1.000 1 2009 2009
dbSNP: rs727504273
rs727504273
3 0.925 0.080 14 23431781 missense variant T/G snv 7.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs886039204
rs886039204
1 14 23423966 missense variant C/T snv 4.0E-06 0.010 1.000 1 2017 2017