Gene: MAPT ×
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: rs17650991
rs17650991
MAPT
2 1.000 0.080 17 45967142 intron variant A/C;G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17651093
rs17651093
MAPT
2 1.000 0.080 17 45972184 intron variant G/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17651134
rs17651134
MAPT
2 1.000 0.080 17 45972974 non coding transcript exon variant G/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17651213
rs17651213
MAPT
3 0.925 0.120 17 45974558 non coding transcript exon variant G/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17651243
rs17651243
MAPT
2 1.000 0.080 17 45974918 non coding transcript exon variant G/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17651285
rs17651285
MAPT
2 1.000 0.080 17 45976871 non coding transcript exon variant G/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17651483
rs17651483
MAPT
2 1.000 0.080 17 45981495 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs17651549
rs17651549
MAPT
4 0.882 0.160 17 45983912 missense variant C/T snv 0.15 0.14 0.700 1.000 1 2012 2012
dbSNP: rs1800547
rs1800547
MAPT
3 0.925 0.120 17 45974480 non coding transcript exon variant A/G snv 0.15 0.14 0.700 1.000 1 2012 2012
dbSNP: rs1864325
rs1864325
MAPT
6 0.882 0.160 17 45900461 intron variant C/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs1981998
rs1981998
MAPT
2 1.000 0.080 17 45979467 non coding transcript exon variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2217394
rs2217394
MAPT
2 1.000 0.080 17 45976082 non coding transcript exon variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs242559
rs242559
MAPT
3 1.000 0.080 17 45948522 intron variant C/A snv 0.71 0.700 1.000 1 2012 2012
dbSNP: rs531217003
rs531217003
MAPT
2 1.000 0.080 17 45986027 intron variant G/A snv 0.700 1.000 1 2012 2012
dbSNP: rs537342897
rs537342897
MAPT
2 1.000 0.080 17 45986842 intron variant G/A snv 0.700 1.000 1 2012 2012
dbSNP: rs541986174
rs541986174
MAPT
2 1.000 0.080 17 45985774 intron variant A/G snv 0.700 1.000 1 2012 2012
dbSNP: rs547435395
rs547435395
MAPT
2 1.000 0.080 17 45986400 intron variant A/G snv 0.700 1.000 1 2012 2012
dbSNP: rs552965964
rs552965964
MAPT
2 1.000 0.080 17 45987393 intron variant A/C snv 0.700 1.000 1 2012 2012
dbSNP: rs571131167
rs571131167
MAPT
2 1.000 0.080 17 45986197 intron variant T/C snv 0.700 1.000 1 2012 2012
dbSNP: rs754512
rs754512
MAPT
2 1.000 0.080 17 45978281 non coding transcript exon variant A/T snv 0.14 0.14 0.700 1.000 1 2012 2012
dbSNP: rs919462
rs919462
MAPT
7 0.807 0.120 17 45988374 intron variant C/T snv 0.15 0.700 1.000 1 2017 2017