Gene: MAPT-AS1 ×
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: rs10445335
rs10445335
MAPT-AS1
1 17 45857530 intron variant T/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs10445364
rs10445364
MAPT-AS1
2 1.000 0.040 17 45838990 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs10445368
rs10445368
MAPT-AS1
2 1.000 0.080 17 45855805 intron variant C/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs10445370
rs10445370
MAPT-AS1
1 17 45857752 intron variant G/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs10491140
rs10491140
MAPT-AS1
1 17 45873610 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1078830
rs1078830
MAPT-AS1
1 17 45868746 intron variant T/C;G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs11079725
rs11079725
SPPL2C ; MAPT-AS1
3 0.925 0.120 17 45846568 synonymous variant T/C snv 0.15 0.14 0.700 1.000 1 2012 2012
dbSNP: rs12150516
rs12150516
MAPT-AS1
1 17 45867153 intron variant C/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs12185233
rs12185233
SPPL2C ; MAPT-AS1
4 0.882 0.160 17 45846288 missense variant G/A;C snv 9.5E-05; 0.15 0.700 1.000 1 2012 2012
dbSNP: rs12185235
rs12185235
SPPL2C ; MAPT-AS1
3 0.925 0.120 17 45846337 synonymous variant C/T snv 0.14 0.14 0.700 1.000 1 2012 2012
dbSNP: rs12185268
rs12185268
SPPL2C ; MAPT-AS1
5 0.851 0.160 17 45846317 missense variant A/G snv 0.15 0.14 0.700 1.000 1 2012 2012
dbSNP: rs12373123
rs12373123
SPPL2C ; MAPT-AS1
4 0.882 0.160 17 45846707 missense variant T/C snv 0.15 0.14 0.700 1.000 1 2012 2012
dbSNP: rs12373124
rs12373124
SPPL2C ; MAPT-AS1
9 0.790 0.120 17 45846853 synonymous variant T/C snv 0.15 0.14 0.700 1.000 1 2012 2012
dbSNP: rs12373139
rs12373139
SPPL2C ; MAPT-AS1
4 0.925 0.120 17 45846764 missense variant G/A snv 0.15 0.14 0.700 1.000 1 2012 2012
dbSNP: rs12373142
rs12373142
SPPL2C ; MAPT-AS1
5 0.851 0.200 17 45846834 missense variant C/G;T snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs12373168
rs12373168
SPPL2C ; MAPT-AS1
2 1.000 0.080 17 45846971 3 prime UTR variant A/C snv 0.16 0.20 0.700 1.000 1 2012 2012
dbSNP: rs1396862
rs1396862
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
2 1.000 0.040 17 45825631 non coding transcript exon variant G/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs16940665
rs16940665
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
2 1.000 0.040 17 45830530 stop lost T/C snv 0.15 0.14 0.700 1.000 1 2012 2012
dbSNP: rs16940674
rs16940674
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
2 1.000 0.040 17 45833141 missense variant C/T snv 0.15 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17689471
rs17689471
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
1 17 45815607 intron variant T/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17689653
rs17689653
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
1 17 45821597 intron variant A/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17689824
rs17689824
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
1 17 45827031 non coding transcript exon variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs17689882
rs17689882
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
2 17 45829462 intron variant G/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17689918
rs17689918
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
6 0.851 0.080 17 45832722 intron variant G/A snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs17690314
rs17690314
MAPT-AS1
1 17 45842518 non coding transcript exon variant T/C;G snv 0.700 1.000 1 2012 2012