Gene: ABCC6 ×
Source: ALL
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: rs1002088882
rs1002088882
ABCC6
4 0.925 0.200 16 16219834 stop gained C/T snv 7.1E-06 0.700 0
dbSNP: rs1006994885
rs1006994885
ABCC6
5 1.000 0.160 16 16150577 splice donor variant C/A;G snv 0.700 0
dbSNP: rs114303883
rs114303883
ABCC6
8 1.000 0.160 16 16182534 stop gained C/A;T snv 9.1E-05 4.2E-05 0.700 0
dbSNP: rs1187315015
rs1187315015
ABCC6 ; LOC105371100
4 1.000 0.160 16 16214323 splice donor variant C/T snv 2.6E-05 3.5E-05 0.700 0
dbSNP: rs1311228469
rs1311228469
ABCC6
4 1.000 0.160 16 16157755 stop gained G/A snv 7.0E-06 0.700 0
dbSNP: rs1333662666
rs1333662666
ABCC6
4 1.000 0.160 16 16150640 stop gained C/A;T snv 4.0E-06 0.700 0
dbSNP: rs1481200467
rs1481200467
ABCC6
7 0.925 0.200 16 16173393 stop gained G/C;T snv 4.0E-06 7.0E-06 0.700 0
dbSNP: rs1555506740
rs1555506740
ABCC6
4 1.000 0.160 16 16150774 splice acceptor variant T/G snv 0.700 0
dbSNP: rs1555507925
rs1555507925
ABCC6
4 1.000 0.160 16 16157768 stop gained C/T snv 0.700 0
dbSNP: rs1555508604
rs1555508604
ABCC6
5 0.925 0.200 16 16161437 splice donor variant C/T snv 0.700 0
dbSNP: rs1555509477
rs1555509477
ABCC6
4 1.000 0.160 16 16165805 missense variant C/T snv 0.700 0
dbSNP: rs1555509485
rs1555509485
ABCC6
3 1.000 0.160 16 16165810 missense variant G/A snv 0.700 0
dbSNP: rs1555512158
rs1555512158
ABCC6
6 0.925 0.200 16 16177554 missense variant C/G snv 0.700 0
dbSNP: rs1555512484
rs1555512484
ABCC6
5 1.000 0.160 16 16178955 missense variant A/G snv 0.700 0
dbSNP: rs1555514895
rs1555514895
ABCC6
3 1.000 0.160 16 16190234 missense variant A/G snv 0.700 0
dbSNP: rs1555523535
rs1555523535
ABCC6
4 0.925 0.200 16 16221822 stop gained G/A snv 0.700 0
dbSNP: rs1555523841
rs1555523841
ABCC6
6 0.882 0.280 16 16223398 splice donor variant C/A snv 0.700 0
dbSNP: rs201766106
rs201766106
ABCC6 ; LOC105371100
5 1.000 0.160 16 16214428 missense variant G/A snv 4.6E-04 3.0E-04 0.700 0
dbSNP: rs28939701
rs28939701
ABCC6
12 0.827 0.240 16 16163087 missense variant G/A snv 4.4E-05 3.5E-05 0.700 0
dbSNP: rs28939702
rs28939702
ABCC6
13 0.851 0.320 16 16154899 missense variant G/A;T snv 8.2E-05 0.700 0
dbSNP: rs369518454
rs369518454
ABCC6
4 0.925 0.200 16 16165721 missense variant C/G;T snv 2.8E-05 0.700 0
dbSNP: rs57794451
rs57794451
ABCC6
3 1.000 0.160 16 16178907 missense variant C/A;T snv 4.0E-06; 2.0E-04 0.700 0
dbSNP: rs59206042
rs59206042
ABCC6
3 1.000 0.160 16 16175918 missense variant G/A;T snv 2.4E-04 0.700 0
dbSNP: rs60791294
rs60791294
ABCC6
11 0.882 0.280 16 16163086 missense variant C/G;T snv 7.6E-05 0.700 0
dbSNP: rs63749796
rs63749796
ABCC6
9 0.925 0.200 16 16159505 missense variant C/G snv 0.700 0