Gene: ARMC2 ×
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: rs11754955
rs11754955
ARMC2
1 6 108966256 intron variant A/G snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs12193858
rs12193858
ARMC2
1 6 108956705 intron variant A/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs12195378
rs12195378
ARMC2
1 6 108963052 intron variant A/G snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs12195728
rs12195728
ARMC2
1 6 108957670 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs12195848
rs12195848
ARMC2
1 6 108957902 intron variant A/C snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs12196010
rs12196010
ARMC2
1 6 108980970 intergenic variant C/A snv 8.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs12196024
rs12196024
ARMC2
1 6 108981055 intergenic variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs12196143
rs12196143
ARMC2
1 6 108981169 intergenic variant C/T snv 9.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs12206834
rs12206834
ARMC2
1 6 108982764 downstream gene variant T/G snv 9.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs12210444
rs12210444
ARMC2
1 6 108984540 downstream gene variant T/C snv 1.0E-01 0.700 1.000 1 2012 2012
dbSNP: rs12212402
rs12212402
ARMC2
1 6 108985478 downstream gene variant T/C snv 9.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs16822
rs16822
SESN1 ; ARMC2
1 6 108986507 3 prime UTR variant G/A snv 9.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs2145763
rs2145763
ARMC2
1 6 108985760 downstream gene variant C/A snv 8.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs3734649
rs3734649
ARMC2
1 6 108973549 3 prime UTR variant C/T snv 0.11 1.0E-01 0.700 1.000 1 2012 2012
dbSNP: rs4509156
rs4509156
SESN1 ; ARMC2
1 6 108987749 intron variant C/A snv 0.11 0.700 1.000 1 2012 2012