Gene: PTCH1 ×
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: rs10512249
rs10512249
PTCH1
2 9 95494027 intron variant G/A snv 0.11 0.700 1.000 1 2010 2010
dbSNP: rs16909859
rs16909859
PTCH1
2 9 95442510 downstream gene variant G/A snv 0.14 0.700 1.000 1 2010 2010
dbSNP: rs16909898
rs16909898
PTCH1 ; LOC100507346
4 9 95468726 intron variant A/G snv 8.4E-02 0.10 0.700 1.000 1 2010 2010
dbSNP: rs2282041
rs2282041
PTCH1
2 9 95486105 intron variant A/G snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs2282043
rs2282043
PTCH1
2 9 95450326 3 prime UTR variant C/T snv 6.5E-02 0.700 1.000 1 2010 2010
dbSNP: rs3824488
rs3824488
PTCH1
2 9 95474382 intron variant C/T snv 6.5E-02 0.700 1.000 1 2010 2010