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: rs387906701
rs387906701
ARHGAP4 ; NAA10
1 1.000 0.080 X 153934388 missense variant A/G snv 0.840 1.000 7 2011 2019
dbSNP: rs863225427
rs863225427
ARHGAP4 ; NAA10
1 1.000 0.080 X 153933994 missense variant T/G snv 0.810 1.000 4 2011 2019
dbSNP: rs1057519448
rs1057519448
ARHGAP4 ; NAA10
1 1.000 0.080 X 153932549 missense variant A/G snv 0.700 1.000 1 2017 2017
dbSNP: rs1557107462
rs1557107462
ARHGAP4 ; NAA10
1 1.000 0.080 X 153932096 missense variant G/C snv 0.700 0
dbSNP: rs1557107528
rs1557107528
ARHGAP4 ; NAA10
2 1.000 0.080 X 153932325 missense variant A/C snv 0.700 0
dbSNP: rs1557107543
rs1557107543
ARHGAP4 ; NAA10
1 1.000 0.080 X 153932398 missense variant C/A snv 0.700 0
dbSNP: rs1569546255
rs1569546255
ARHGAP4 ; NAA10
1 1.000 0.080 X 153930200 frameshift variant TT/- delins 0.700 0
dbSNP: rs587780562
rs587780562
ARHGAP4 ; NAA10
1 1.000 0.080 X 153932338 missense variant C/A snv 0.700 0
dbSNP: rs587780563
rs587780563
ARHGAP4 ; NAA10
1 1.000 0.080 X 153932111 missense variant G/A snv 0.700 0
dbSNP: rs797044868
rs797044868
ARHGAP4 ; NAA10
1 1.000 0.080 X 153932410 missense variant G/A snv 0.700 0
dbSNP: rs878853263
rs878853263
ARHGAP4 ; NAA10
1 1.000 0.080 X 153932073 missense variant A/C;T snv 0.700 0
dbSNP: rs878853264
rs878853264
ARHGAP4 ; NAA10
2 1.000 0.080 X 153932075 missense variant A/T snv 0.700 0