RYR3, ryanodine receptor 3, 6263

N. diseases: 40; N. variants: 9
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: rs11072541
rs11072541 		0.925 0.040 15 33555179 intron variant G/A snv 2.7E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs16973282
rs16973282 		0.925 0.040 15 33614399 intron variant A/G snv 5.5E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018