Gene: CNIH3 ×
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: rs1532557
rs1532557
CNIH3 ; CNIH3-AS2
1 1 224617410 intron variant C/T snv 0.27 0.700 1.000 1 2017 2017
dbSNP: rs16841702
rs16841702
CNIH3
1 1 224565435 non coding transcript exon variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs1891243
rs1891243
CNIH3
1 1 224499743 intron variant G/A snv 0.51 0.700 1.000 1 2017 2017
dbSNP: rs4654049
rs4654049
CNIH3
1 1 224585208 intron variant C/T snv 0.39 0.700 1.000 1 2017 2017
dbSNP: rs6426142
rs6426142
CNIH3
1 1 224580550 intron variant T/C snv 0.16 0.700 1.000 1 2017 2017
dbSNP: rs6695773
rs6695773
CNIH3
1 1 224516534 intron variant T/G snv 0.27 0.700 1.000 1 2017 2017
dbSNP: rs712068
rs712068
CNIH3
1 1 224525862 intron variant A/G snv 0.32 0.700 1.000 1 2017 2017
dbSNP: rs7550648
rs7550648
CNIH3
1 1 224519475 intron variant C/T snv 0.23 0.700 1.000 1 2017 2017
dbSNP: rs880496
rs880496
CNIH3
1 1 224620432 intron variant G/T snv 0.15 0.700 1.000 1 2017 2017
dbSNP: rs883115
rs883115
CNIH3
1 1 224619859 intron variant T/A;C snv 0.700 1.000 1 2017 2017