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: rs4988235
rs4988235
MCM6
19 0.752 0.400 2 135851076 intron variant G/A;C snv 0.800 0.941 17 2009 2019
dbSNP: rs145946881
rs145946881
MCM6
1 2 135851176 intron variant C/G;T snv 0.710 1.000 1 2017 2017
dbSNP: rs41380347
rs41380347
MCM6
1 2 135851081 intron variant A/C;G snv 0.710 1.000 1 2017 2017
dbSNP: rs41525747
rs41525747
MCM6
1 2 135851073 intron variant G/C snv 3.5E-05 0.710 1.000 1 2017 2017
dbSNP: rs182549
rs182549
MCM6
4 2 135859184 intron variant C/T snv 0.41 0.700 0
dbSNP: rs1220047339
rs1220047339
GLB1 ; LOC107986073
1 3 33018492 missense variant G/A snv 0.010 1.000 1 2008 2008
dbSNP: rs309180
rs309180
MCM6
2 2 135856685 intron variant G/A snv 0.54 0.50 0.010 < 0.001 1 2016 2016
dbSNP: rs3754686
rs3754686
MCM6
2 2 135845706 intron variant T/C snv 0.51 0.010 1.000 1 2016 2016
dbSNP: rs869051967
rs869051967
MCM6
1 2 135851175 intron variant A/C snv 3.5E-05 0.010 1.000 1 2017 2017