Gene: CCDC171 ×
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: rs4740619
rs4740619
CCDC171
1 9 15634328 intron variant T/A;C snv 0.700 1.000 5 2015 2019
dbSNP: rs13292699
rs13292699
CCDC171
1 9 15910046 intron variant A/C snv 0.34 0.700 1.000 1 2019 2019
dbSNP: rs1539172
rs1539172
CCDC171 ; LOC107987049
1 9 15784633 missense variant A/G snv 0.47 0.50 0.700 1.000 1 2018 2018
dbSNP: rs770214
rs770214
CCDC171
1 9 15888708 intron variant G/A snv 0.81 0.700 1.000 1 2018 2018