Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121434578
rs121434578
1.000 0.080 16 8768248 missense variant G/A snv
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 1.000 1 2010 2010
dbSNP: rs724159992
rs724159992
1.000 0.080 16 8750498 missense variant G/A snv 1.4E-05
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 1.000 1 2010 2010
dbSNP: rs724159990
rs724159990
1.000 0.080 16 8768220 missense variant C/T snv
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 0
dbSNP: rs724159991
rs724159991
1.000 0.080 16 8781360 missense variant T/C snv
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 1.000 1 2010 2010
dbSNP: rs763028380
rs763028380
0.851 0.320 11 17453271 missense variant C/A;G;T snv 4.0E-06; 1.6E-05
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 0
dbSNP: rs1131692228
rs1131692228
0.925 0.160 7 100646637 missense variant C/T snv
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 0
dbSNP: rs1057518345
rs1057518345
0.742 0.400 20 50894172 frameshift variant ACTA/- delins
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 0
dbSNP: rs1131692272
rs1131692272
0.851 0.240 2 100006808 missense variant C/T snv
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 0
dbSNP: rs1554699491
rs1554699491
0.763 0.280 9 85596450 splice acceptor variant C/A snv
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 0
dbSNP: rs780631499
rs780631499
0.763 0.280 9 85588465 frameshift variant G/- del 4.0E-06 7.0E-06
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 0
dbSNP: rs794727931
rs794727931
0.790 0.240 11 78112692 missense variant A/C snv
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 0
dbSNP: rs1557612048
rs1557612048
0.807 0.200 1 26767868 missense variant T/C snv
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 0
dbSNP: rs797045283
rs797045283
0.827 0.320 6 157207109 stop gained C/T snv
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 0
dbSNP: rs1057518794
rs1057518794
ARX
X 25004777 frameshift variant TCTG/- delins
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 0
dbSNP: rs377619533
rs377619533
1.000 18 33743312 stop gained C/A;T snv 2.8E-05
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 0
dbSNP: rs1057516032
rs1057516032
1.000 19 41970211 protein altering variant AGTCT/GA delins
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 1.000 1 2016 2016
dbSNP: rs867410737
rs867410737
0.708 0.440 19 1242559 missense variant C/T snv 6.7E-06
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 1.000 1 2018 2018
dbSNP: rs72554640
rs72554640
0.882 0.160 X 78011239 stop gained C/T snv
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 0
dbSNP: rs1557106484
rs1557106484
X 77633315 missense variant C/A snv
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 0
dbSNP: rs1135401778
rs1135401778
0.752 0.400 17 67854315 frameshift variant T/- del
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 1.000 1 2017 2017
dbSNP: rs1425998598
rs1425998598
0.763 0.240 17 67918802 missense variant G/A;C snv 1.2E-05
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 1.000 1 2017 2017
dbSNP: rs1555639076
rs1555639076
0.790 0.400 17 67893677 splice donor variant A/- delins
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 1.000 1 2017 2017
dbSNP: rs1555639411
rs1555639411
0.790 0.360 17 67894102 frameshift variant -/G delins
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 1.000 1 2017 2017
dbSNP: rs1057519429
rs1057519429
0.807 0.240 19 13235666 missense variant C/G;T snv
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 0
dbSNP: rs1555736565
rs1555736565
0.925 0.080 19 13230191 missense variant C/A;T snv
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 0