Gene: PRRC2A ×
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: rs2260000
rs2260000
PRRC2A
7 0.851 0.200 6 31625699 intron variant A/G snv 0.29 0.700 1.000 3 2007 2011
dbSNP: rs2261033
rs2261033
PRRC2A
3 0.925 0.160 6 31635814 non coding transcript exon variant A/G snv 0.42 0.700 1.000 3 2007 2011
dbSNP: rs3115663
rs3115663
PRRC2A ; MIR6832
7 0.827 0.360 6 31634066 non coding transcript exon variant T/C snv 0.17 0.700 1.000 3 2007 2011
dbSNP: rs11229
rs11229
PRRC2A
6 0.851 0.280 6 31635993 synonymous variant A/G snv 0.14 0.17 0.700 1.000 2 2007 2009
dbSNP: rs1046080
rs1046080
PRRC2A
2 1.000 0.120 6 31628105 missense variant C/A snv 0.79 0.74 0.700 1.000 1 2011 2011
dbSNP: rs2272593
rs2272593
PRRC2A ; MIR6832
1 1.000 0.120 6 31633567 missense variant T/C snv 0.79 0.74 0.700 1.000 1 2011 2011
dbSNP: rs2736155
rs2736155
PRRC2A
2 0.925 0.160 6 31637422 non coding transcript exon variant G/C snv 0.51 0.44 0.700 1.000 1 2011 2011
dbSNP: rs2736157
rs2736157
PRRC2A ; MIR6832
2 1.000 0.120 6 31633043 intron variant A/G;T snv 0.15 0.17 0.700 1.000 1 2011 2011
dbSNP: rs2736171
rs2736171
PRRC2A
5 0.925 0.120 6 31627710 intron variant A/G snv 0.34 0.700 1.000 1 2011 2011
dbSNP: rs2736172
rs2736172
PRRC2A ; SNORA38
6 0.882 0.160 6 31623121 non coding transcript exon variant C/T snv 0.41 0.29 0.700 1.000 1 2011 2011
dbSNP: rs2736176
rs2736176
PRRC2A
1 1.000 0.120 6 31619784 upstream gene variant G/A;C snv 0.23 0.700 1.000 1 2011 2011
dbSNP: rs2844472
rs2844472
PRRC2A ; SNORA38
5 0.925 0.120 6 31621899 intron variant A/G snv 0.29 0.700 1.000 1 2011 2011
dbSNP: rs2857693
rs2857693
PRRC2A
2 1.000 0.120 6 31620607 upstream gene variant G/T snv 0.33 0.700 1.000 1 2011 2011
dbSNP: rs3130626
rs3130626
PRRC2A
2 1.000 0.120 6 31630712 synonymous variant A/G snv 0.15 0.17 0.700 1.000 1 2011 2011
dbSNP: rs3132450
rs3132450
PRRC2A
1 1.000 0.120 6 31628361 intron variant A/G snv 7.1E-02 0.700 1.000 1 2011 2011