RHAG, Rh associated glycoprotein, 6005

N. diseases: 41; N. variants: 13
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: rs863225468
rs863225468
1.000 0.120 6 49619326 missense variant A/G snv
CUI: C1861455
Disease: STOMATOCYTOSIS I
STOMATOCYTOSIS I
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.810 1.000 3 2009 2012
dbSNP: rs863225469
rs863225469
0.925 0.120 6 49619338 missense variant A/C snv
CUI: C1861455
Disease: STOMATOCYTOSIS I
STOMATOCYTOSIS I
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.810 1.000 3 2009 2012
dbSNP: rs1554174425
rs1554174425
0.925 0.160 6 49618113 missense variant A/C snv
CUI: C1861455
Disease: STOMATOCYTOSIS I
STOMATOCYTOSIS I
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.700 0