Gene: LINC02210-CRHR1 ×
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: rs12938031
rs12938031
LINC02210-CRHR1
6 0.851 0.160 17 45777136 intron variant A/G snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs1724422
rs1724422
LINC02210-CRHR1
2 1.000 0.040 17 45699947 intron variant A/G snv 0.47 0.700 1.000 1 2018 2018
dbSNP: rs34186148
rs34186148
LINC02210-CRHR1
2 1.000 0.040 17 45777289 intron variant G/A;C snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs35909029
rs35909029
LINC02210-CRHR1
2 1.000 0.040 17 45774132 intron variant T/A;C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs62057061
rs62057061
LINC02210-CRHR1
2 1.000 0.040 17 45779273 intron variant C/G snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs7225384
rs7225384
LINC02210-CRHR1 ; LOC107985028
2 1.000 0.040 17 45731730 non coding transcript exon variant C/G snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs9303521
rs9303521
LINC02210-CRHR1
5 0.925 0.120 17 45727828 intron variant T/C;G snv 0.60 0.700 1.000 1 2018 2018
dbSNP: rs16940655
rs16940655
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
1 17 45816520 missense variant C/A;T snv 4.0E-06; 6.4E-03 0.010 1.000 1 2013 2013
dbSNP: rs4076452
rs4076452
LINC02210-CRHR1
2 1.000 0.040 17 45778528 intron variant G/C snv 0.16 0.010 1.000 1 2013 2013