Gene: CCDC162P ×
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: rs9386791
rs9386791
CCDC162P
2 6 109287294 intron variant C/T snv 0.51 0.700 1.000 2 2012 2013
dbSNP: rs1006081
rs1006081
CCDC162P
1 6 109304347 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs1008084
rs1008084
CCDC162P
3 6 109305762 intron variant G/A snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs1111863
rs1111863
CCDC162P ; PTCHD3P3
1 6 109290003 non coding transcript exon variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1111865
rs1111865
CCDC162P ; PTCHD3P3
1 6 109289660 intron variant C/T snv 0.51 0.700 1.000 1 2012 2012
dbSNP: rs1111866
rs1111866
CCDC162P ; PTCHD3P3
1 6 109289643 intron variant G/T snv 0.51 0.700 1.000 1 2012 2012
dbSNP: rs11153165
rs11153165
CCDC162P
1 6 109300956 intron variant G/A snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs11153166
rs11153166
CCDC162P
1 6 109301291 intron variant A/G snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs11153167
rs11153167
CCDC162P
1 6 109301379 intron variant A/T snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs11153168
rs11153168
CCDC162P
1 6 109308217 non coding transcript exon variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11153169
rs11153169
CCDC162P
1 6 109322318 intron variant G/T snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs11759269
rs11759269
CCDC162P
1 6 109319285 intron variant A/G snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs11962354
rs11962354
CCDC162P
1 6 109174989 intron variant C/T snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs11964178
rs11964178
CCDC162P
1 6 109240832 intron variant A/G snv 0.48 0.700 1.000 1 2012 2012
dbSNP: rs12191774
rs12191774
CCDC162P
1 6 109327150 intron variant A/G snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs12200757
rs12200757
CCDC162P
1 6 109330017 intron variant C/T snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs12528712
rs12528712
CCDC162P ; LOC101927538
1 6 109339681 intron variant C/A snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs1260593
rs1260593
CCDC162P
1 6 109200197 intron variant C/T snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs1260595
rs1260595
CCDC162P
1 6 109198670 intron variant T/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs1260596
rs1260596
CCDC162P
1 6 109198644 intron variant T/C snv 0.53 0.700 1.000 1 2012 2012
dbSNP: rs12660449
rs12660449
CCDC162P
1 6 109203592 intron variant G/A snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs13190802
rs13190802
CCDC162P
1 6 109260601 intron variant G/A snv 9.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs13196219
rs13196219
CCDC162P
1 6 109314584 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs13196590
rs13196590
CCDC162P
1 6 109240715 intron variant T/C snv 0.39 0.700 1.000 1 2012 2012
dbSNP: rs13199388
rs13199388
CCDC162P
1 6 109262897 intron variant C/T snv 9.6E-02 0.700 1.000 1 2012 2012