Gene: HCRTR2 ×
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: rs3122163
rs3122163
HCRTR2
2 6 55191570 intron variant C/T snv 0.85 0.700 1.000 1 2017 2017
dbSNP: rs35833281
rs35833281
HCRTR2
1 6 55156763 intron variant G/C snv 0.15 0.700 1.000 1 2016 2016
dbSNP: rs76899638
rs76899638
HCRTR2
1 6 55282710 downstream gene variant -/GT delins 0.83 0.700 1.000 1 2016 2016