Gene: CCDC12 ×
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: rs13092573
rs13092573
CCDC12
2 3 46947071 intron variant C/T snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs7628747
rs7628747
CCDC12
1 3 46960500 intron variant A/T snv 0.49 0.700 1.000 1 2018 2018