Gene: TNFRSF11B ×
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: rs11573829
rs11573829
TNFRSF11B
1 8 118947384 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs11573885
rs11573885
TNFRSF11B
1 8 118936926 intron variant T/C snv 0.45 0.700 1.000 1 2009 2009
dbSNP: rs1485289
rs1485289
TNFRSF11B
1 8 118942040 intron variant G/A snv 0.60 0.700 1.000 1 2009 2009
dbSNP: rs1905786
rs1905786
TNFRSF11B
2 1.000 0.040 8 118939453 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs2073617
rs2073617
TNFRSF11B ; COLEC10
9 0.776 0.360 8 118952044 upstream gene variant G/A snv 0.58 0.700 1.000 1 2009 2009
dbSNP: rs2073618
rs2073618
TNFRSF11B ; COLEC10
19 0.716 0.480 8 118951813 missense variant G/C snv 0.52 0.60 0.700 1.000 1 2009 2009
dbSNP: rs3134063
rs3134063
TNFRSF11B
1 8 118947418 intron variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs4319131
rs4319131
TNFRSF11B
1 8 118935412 intron variant A/G snv 0.33 0.700 1.000 1 2009 2009
dbSNP: rs6415470
rs6415470
TNFRSF11B
1 8 118942872 intron variant G/A snv 0.67 0.700 1.000 1 2009 2009
dbSNP: rs6469788
rs6469788
TNFRSF11B
1 8 118940511 intron variant A/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs6469789
rs6469789
TNFRSF11B
1 8 118948422 intron variant C/A;G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs7010267
rs7010267
TNFRSF11B
1 8 118934417 intron variant C/A snv 0.38 0.700 1.000 1 2018 2018
dbSNP: rs7463176
rs7463176
TNFRSF11B
1 8 118945386 intron variant A/C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs7464496
rs7464496
TNFRSF11B
1 8 118942603 intron variant T/C snv 0.60 0.700 1.000 1 2009 2009