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: rs1057519838
rs1057519838
0.882 0.160 5 68293790 stop gained C/T snv
CUI: C4014934
Disease: IMMUNODEFICIENCY 36
IMMUNODEFICIENCY 36
0.700 0
dbSNP: rs1057519838
rs1057519838
0.882 0.160 5 68293790 stop gained C/T snv
CUI: C0878684
Disease: SHORT syndrome
SHORT syndrome
0.700 0
dbSNP: rs1057519838
rs1057519838
0.882 0.160 5 68293790 stop gained C/T snv
AGAMMAGLOBULINEMIA 7, AUTOSOMAL RECESSIVE
0.700 0
dbSNP: rs1554051033
rs1554051033
1.000 5 68293708 splice acceptor variant G/C snv
CUI: C4014934
Disease: IMMUNODEFICIENCY 36
IMMUNODEFICIENCY 36
0.700 0
dbSNP: rs1554051067
rs1554051067
1.000 5 68293835 splice donor variant TG/- delins
CUI: C4014934
Disease: IMMUNODEFICIENCY 36
IMMUNODEFICIENCY 36
0.700 0
dbSNP: rs1554051075
rs1554051075
1.000 5 68293836 splice donor variant T/A;G snv
CUI: C4014934
Disease: IMMUNODEFICIENCY 36
IMMUNODEFICIENCY 36
0.700 0
dbSNP: rs397509384
rs397509384
1.000 5 68280983 stop gained G/A snv
AGAMMAGLOBULINEMIA 7, AUTOSOMAL RECESSIVE
0.700 0
dbSNP: rs398122384
rs398122384
1.000 0.160 5 68296298 frameshift variant -/T delins
CUI: C0878684
Disease: SHORT syndrome
SHORT syndrome
0.700 0
dbSNP: rs398122385
rs398122385
1.000 0.160 5 68296262 frameshift variant -/C ins
CUI: C0878684
Disease: SHORT syndrome
SHORT syndrome
0.700 0
dbSNP: rs515726149
rs515726149
1.000 0.160 5 68296248 missense variant G/A snv
CUI: C0878684
Disease: SHORT syndrome
SHORT syndrome
0.700 0
dbSNP: rs515726150
rs515726150
1.000 0.160 5 68296260 frameshift variant AA/- delins
CUI: C0878684
Disease: SHORT syndrome
SHORT syndrome
0.700 0
dbSNP: rs515726151
rs515726151
1.000 0.160 5 68296327 stop gained T/G snv
CUI: C0878684
Disease: SHORT syndrome
SHORT syndrome
0.700 0
dbSNP: rs587784325
rs587784325
1.000 0.160 5 68293187 missense variant C/T snv
CUI: C0878684
Disease: SHORT syndrome
SHORT syndrome
0.700 0
dbSNP: rs1057519757
rs1057519757
0.882 0.120 5 68293310 missense variant G/A;C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 2 2010 2014
dbSNP: rs587777709
rs587777709
0.882 0.160 5 68293835 splice donor variant G/A;C;T snv
CUI: C4014934
Disease: IMMUNODEFICIENCY 36
IMMUNODEFICIENCY 36
0.700 1.000 4 2012 2016
dbSNP: rs587777709
rs587777709
0.882 0.160 5 68293835 splice donor variant G/A;C;T snv
CUI: C0878684
Disease: SHORT syndrome
SHORT syndrome
0.700 1.000 4 2012 2016
dbSNP: rs587777709
rs587777709
0.882 0.160 5 68293835 splice donor variant G/A;C;T snv
AGAMMAGLOBULINEMIA 7, AUTOSOMAL RECESSIVE
0.700 1.000 4 2012 2016
dbSNP: rs397515453
rs397515453
0.752 0.440 5 68296301 missense variant C/T snv
AGAMMAGLOBULINEMIA 7, AUTOSOMAL RECESSIVE
0.700 1.000 9 2013 2017
dbSNP: rs397515453
rs397515453
0.752 0.440 5 68296301 missense variant C/T snv
CUI: C4014934
Disease: IMMUNODEFICIENCY 36
IMMUNODEFICIENCY 36
0.700 1.000 9 2013 2017
dbSNP: rs397515453
rs397515453
0.752 0.440 5 68296301 missense variant C/T snv
CUI: C0878684
Disease: SHORT syndrome
SHORT syndrome
0.820 1.000 9 2013 2018
dbSNP: rs1561299903
rs1561299903
0.882 0.160 5 68295287 frameshift variant -/T delins
CUI: C4014934
Disease: IMMUNODEFICIENCY 36
IMMUNODEFICIENCY 36
0.700 1.000 3 2013 2014
dbSNP: rs1561299903
rs1561299903
0.882 0.160 5 68295287 frameshift variant -/T delins
CUI: C0878684
Disease: SHORT syndrome
SHORT syndrome
0.700 1.000 3 2013 2014
dbSNP: rs1561299903
rs1561299903
0.882 0.160 5 68295287 frameshift variant -/T delins
AGAMMAGLOBULINEMIA 7, AUTOSOMAL RECESSIVE
0.700 1.000 3 2013 2014
dbSNP: rs397514047
rs397514047
1.000 0.160 5 68294575 missense variant G/A snv
CUI: C0878684
Disease: SHORT syndrome
SHORT syndrome
0.800 1.000 1 2013 2013
dbSNP: rs773686816
rs773686816
5 68295271 missense variant C/A;G;T snv 4.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 2 2014 2014