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: rs10836955
rs10836955
MMP26 ; OR51G1
1 11 4924401 intron variant G/A snv 0.15 0.700 1.000 1 2008 2008
dbSNP: rs10837104
rs10837104
OR51L1
1 11 4997987 intron variant C/G snv 0.30 0.700 1.000 1 2008 2008
dbSNP: rs10837107
rs10837107
OR51L1
1 11 4998127 intron variant T/C snv 0.29 0.700 1.000 1 2008 2008
dbSNP: rs10837108
rs10837108
OR51L1
1 11 4998887 5 prime UTR variant C/G;T snv 0.700 1.000 1 2008 2008
dbSNP: rs10837513
rs10837513
OR52Z1
1 11 5179410 upstream gene variant G/T snv 0.70 0.700 1.000 1 2008 2008
dbSNP: rs10837593
rs10837593 		1 11 5210667 downstream gene variant C/T snv 0.79 0.700 1.000 1 2008 2008
dbSNP: rs10837767
rs10837767
HBE1 ; HBG2
1 11 5296323 intron variant T/G snv 0.51 0.700 1.000 1 2008 2008
dbSNP: rs10838245
rs10838245
UBQLNL
1 11 5514299 intron variant G/A;C;T snv 0.700 1.000 1 2008 2008
dbSNP: rs10838807
rs10838807
OR52Q1P ; TRIM5 ; LOC112268071
1 11 5904419 non coding transcript exon variant G/T snv 9.2E-02 0.700 1.000 1 2008 2008
dbSNP: rs11030841
rs11030841
STIM1
1 11 4077783 intron variant A/G;T snv 0.700 1.000 1 2008 2008
dbSNP: rs11035045
rs11035045 		1 11 4994711 upstream gene variant C/T snv 0.33 0.700 1.000 1 2008 2008
dbSNP: rs11035046
rs11035046
OR51L1
1 11 4995039 5 prime UTR variant G/A snv 0.33 0.700 1.000 1 2008 2008
dbSNP: rs11035064
rs11035064
OR51L1
1 11 4998959 5 prime UTR variant C/T snv 0.25 0.29 0.700 1.000 1 2008 2008
dbSNP: rs11036238
rs11036238 		2 1.000 0.040 11 5204405 upstream gene variant G/C snv 0.21 0.700 1.000 1 2008 2008
dbSNP: rs11037191
rs11037191
HBE1 ; HBG2 ; OR51B5 ; OR51M1
1 11 5390842 3 prime UTR variant A/G snv 4.6E-02 0.700 1.000 1 2008 2008
dbSNP: rs11037417
rs11037417
HBE1 ; HBG2 ; OR51B5
1 11 5427313 intron variant G/A snv 0.24 0.700 1.000 1 2008 2008
dbSNP: rs11037444
rs11037444
HBE1 ; HBG2 ; OR51B5 ; OR51I1
1 11 5440855 synonymous variant G/A snv 0.21 0.19 0.700 1.000 1 2008 2008
dbSNP: rs11037866
rs11037866
HBE1 ; HBG2 ; OR51B5
1 11 5504641 intron variant C/T snv 0.26 0.700 1.000 1 2008 2008
dbSNP: rs11039100
rs11039100
TRIM5 ; OR52N2
2 11 5805773 intron variant T/C snv 0.11 0.700 1.000 1 2008 2008
dbSNP: rs11039101
rs11039101
TRIM5 ; OR52N2
1 11 5805850 intron variant G/A snv 0.11 0.700 1.000 1 2008 2008
dbSNP: rs11039164
rs11039164
TRIM5 ; OR52N2
1 11 5821908 intron variant G/A snv 0.10 0.700 1.000 1 2008 2008
dbSNP: rs11039274
rs11039274
TRIM5
1 11 5845723 intron variant T/G snv 6.2E-02 0.700 1.000 1 2008 2008
dbSNP: rs11039351
rs11039351
TRIM5
1 11 5864616 intron variant C/T snv 6.2E-02 0.700 1.000 1 2008 2008
dbSNP: rs11039508
rs11039508
TRIM5 ; OR52E5 ; LOC112268071
1 11 5899467 intron variant A/G snv 6.5E-02 0.700 1.000 1 2008 2008
dbSNP: rs11125841
rs11125841
LOC102724142
1 2 60400430 intron variant A/G snv 0.48 0.700 1.000 1 2007 2007