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: rs121918007
rs121918007
ALPL
4 0.851 0.080 1 21564139 missense variant G/A;C snv 2.4E-03; 4.0E-06 0.710 1.000 6 1992 2014
dbSNP: rs121918001
rs121918001
ALPL
3 0.882 0.080 1 21561126 missense variant C/A;T snv 0.700 1.000 1 2001 2001
dbSNP: rs1442918125
rs1442918125
ALPL
2 0.925 0.080 1 21575907 missense variant G/A snv 8.0E-06 7.0E-06 0.700 1.000 1 2001 2001
dbSNP: rs121918002
rs121918002
ALPL
4 0.851 0.080 1 21573683 missense variant A/C snv 3.6E-05 7.0E-05 0.700 0
dbSNP: rs121918008
rs121918008
ALPL
4 0.851 0.080 1 21575868 missense variant A/T snv 4.0E-06 7.0E-06 0.700 0
dbSNP: rs121918009
rs121918009
ALPL
4 0.851 0.080 1 21575736 missense variant G/A snv 0.700 0
dbSNP: rs121918011
rs121918011
ALPL
4 0.851 0.080 1 21563219 missense variant G/A;C snv 1.4E-04 0.700 0
dbSNP: rs121918013
rs121918013
ALPL
5 0.827 0.120 1 21563158 missense variant G/A snv 0.700 0
dbSNP: rs121918018
rs121918018
ALPL
3 0.882 0.120 1 21568201 missense variant G/C;T snv 1.6E-05; 4.0E-06 0.700 0
dbSNP: rs121918019
rs121918019
ALPL
3 0.882 0.080 1 21564094 missense variant G/A;C snv 9.2E-05 0.700 0
dbSNP: rs121918020
rs121918020
ALPL
2 0.925 0.080 1 21570326 missense variant C/T snv 1.6E-05 1.4E-05 0.700 0
dbSNP: rs1237252052
rs1237252052
ALPL
1 1.000 0.080 1 21570336 missense variant T/C snv 4.0E-06 0.700 0
dbSNP: rs1413274209
rs1413274209
ALPL
3 0.882 0.080 1 21577544 missense variant G/A snv 8.3E-06 2.1E-05 0.700 0
dbSNP: rs199669988
rs199669988
ALPL
3 0.882 0.080 1 21564097 missense variant G/A snv 1.3E-04 3.5E-05 0.700 0
dbSNP: rs371243939
rs371243939
ALPL
3 0.882 0.080 1 21575906 missense variant C/T snv 1.2E-05 1.4E-05 0.700 0
dbSNP: rs766076920
rs766076920
ALPL
3 0.882 0.080 1 21568122 missense variant C/T snv 8.0E-06 2.1E-05 0.700 0
dbSNP: rs786204530
rs786204530
ALPL
4 0.851 0.160 1 21563212 missense variant AC/CA mnv 0.700 0