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: rs104893674
rs104893674
ZAP70
2 0.925 0.120 2 97737828 missense variant C/A snv 0.700 1.000 5 1994 2009
dbSNP: rs137853201
rs137853201
ZAP70
2 0.925 0.120 2 97737577 missense variant G/A snv 4.0E-06 0.700 1.000 5 1994 2009
dbSNP: rs113994172
rs113994172
ZAP70
1 1.000 0.120 2 97724275 missense variant C/A snv 0.700 0
dbSNP: rs113994173
rs113994173
ZAP70
1 1.000 0.120 2 97733464 non coding transcript exon variant G/A snv 0.700 0
dbSNP: rs113994174
rs113994174
ZAP70
1 1.000 0.120 2 97737576 missense variant C/T snv 8.0E-06 1.4E-05 0.700 0
dbSNP: rs113994175
rs113994175
ZAP70
1 1.000 0.120 2 97738085 missense variant A/T snv 0.700 0
dbSNP: rs1254428002
rs1254428002
ZAP70
1 1.000 0.120 2 97734640 missense variant T/G snv 7.0E-06 0.700 0
dbSNP: rs1559328006
rs1559328006
ZAP70
1 1.000 0.120 2 97735413 frameshift variant -/T delins 0.700 0