Gene: LINC02210-CRHR1 ×
Source: GWASDB ×
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: rs2942168
rs2942168
LINC02210 ; LINC02210-CRHR1
3 0.925 0.120 17 45637484 non coding transcript exon variant G/A;C;T snv 0.14 0.820 1.000 3 2011 2014
dbSNP: rs393152
rs393152
LINC02210 ; LINC02210-CRHR1
5 0.851 0.160 17 45641777 non coding transcript exon variant A/G snv 0.18 0.29 0.810 1.000 3 2009 2015
dbSNP: rs417968
rs417968
LINC02210 ; LINC02210-CRHR1
2 1.000 0.040 17 45651010 non coding transcript exon variant G/A snv 0.65 0.700 1.000 5 2009 2014
dbSNP: rs7215239
rs7215239
LINC02210-CRHR1
3 1.000 0.040 17 45690407 intron variant T/C snv 0.30 0.700 1.000 4 2011 2014
dbSNP: rs1526123
rs1526123
LINC02210-CRHR1
1 1.000 0.040 17 45705974 intron variant T/C snv 0.55 0.700 1.000 2 2009 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 2 2011 2012
dbSNP: rs1876828
rs1876828
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
1 0.851 0.160 17 45834159 intron variant C/T snv 0.14 0.700 1.000 2 2011 2012
dbSNP: rs4525537
rs4525537
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
1 1.000 0.040 17 45835357 3 prime UTR variant T/C snv 0.14 0.700 1.000 2 2011 2012
dbSNP: rs878887
rs878887
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
2 1.000 0.040 17 45835216 3 prime UTR variant C/T snv 0.14 0.700 1.000 2 2011 2012
dbSNP: rs878888
rs878888
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
1 1.000 0.040 17 45835269 3 prime UTR variant A/G snv 0.14 0.700 1.000 2 2011 2012
dbSNP: rs12150390
rs12150390
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
1 1.000 0.040 17 45818862 intron variant T/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs12938476
rs12938476
LINC02210-CRHR1 ; LOC107985028
1 1.000 0.040 17 45735531 intron variant T/C snv 0.40 0.700 1.000 1 2011 2011
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: rs1635291
rs1635291
LINC02210-CRHR1
2 1.000 0.040 17 45674547 intron variant G/A snv 0.69 0.700 1.000 1 2011 2011
dbSNP: rs16940668
rs16940668
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
1 1.000 0.040 17 45830600 non coding transcript exon variant G/A snv 0.15 0.14 0.700 1.000 1 2011 2011
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 2011 2011
dbSNP: rs16940676
rs16940676
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
1 1.000 0.040 17 45833670 intron variant G/A snv 0.14 0.14 0.700 1.000 1 2011 2011
dbSNP: rs16940677
rs16940677
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
1 1.000 0.040 17 45834532 intron variant C/T snv 0.14 0.700 1.000 1 2014 2014
dbSNP: rs17334797
rs17334797
LINC02210-CRHR1
2 1.000 0.040 17 45748546 intron variant A/G snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs17425752
rs17425752
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
1 1.000 0.040 17 45829360 splice region variant A/C snv 0.15 0.14 0.700 1.000 1 2011 2011
dbSNP: rs17426064
rs17426064
LINC02210-CRHR1
2 1.000 0.040 17 45751332 intron variant C/T snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs17763086
rs17763086
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
2 1.000 0.040 17 45828115 intron variant T/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs1876829
rs1876829
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
2 1.000 0.040 17 45834077 intron variant T/C snv 0.15 0.14 0.700 1.000 1 2011 2011
dbSNP: rs1876830
rs1876830
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
1 1.000 0.040 17 45833986 intron variant C/T snv 0.15 0.14 0.700 1.000 1 2011 2011
dbSNP: rs1912151
rs1912151
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
2 1.000 0.040 17 45825578 splice region variant C/T snv 0.25 0.14 0.700 1.000 1 2012 2012