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: rs10040979
rs10040979
EBF1
1 5 158997383 intron variant G/A snv 0.61 0.700 1.000 1 2013 2013
dbSNP: rs11651483
rs11651483
ARHGAP44
1 17 12874085 intron variant A/G snv 0.76 0.700 1.000 1 2013 2013
dbSNP: rs4235898
rs4235898
LINC02540
1 6 76556471 intron variant G/A snv 0.70 0.700 1.000 1 2013 2013
dbSNP: rs4771859
rs4771859
GPC5
1 13 92436398 intron variant T/C snv 0.62 0.700 1.000 1 2013 2013