SCIN, scinderin, 85477

N. diseases: 36; N. variants: 2
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs17166189
rs17166189 		0.925 0.040 7 12579299 intron variant T/G snv 3.9E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018