Gene: CCDC192 ×
Source: INFERRED ×
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: rs2764766
rs2764766
CCDC192
1 1.000 0.040 5 127877933 intron variant C/G snv 0.66 0.700 1.000 2 2017 2019
dbSNP: rs245201
rs245201
CCDC192
1 1.000 0.040 5 127833520 intron variant A/G snv 0.29 0.700 1.000 1 2009 2009