ClinVar Miner

List of variants in gene ORAI1 reported as likely benign for immune system disorder

Included ClinVar conditions (908):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_032790.4(ORAI1):c.668A>G (p.Asn223Ser) rs75603737 0.00127
NM_032790.4(ORAI1):c.763G>A (p.Val255Ile) rs376286032 0.00014
NM_032790.4(ORAI1):c.735C>T (p.Pro245=) rs370588656 0.00013
NM_032790.3(ORAI1):c.309-4G>A rs371157536 0.00009
NC_000012.12:g.121641430G>A rs200214435 0.00008
NC_000012.12:g.121641067C>T rs375801854 0.00004
NM_032790.4(ORAI1):c.540C>T (p.Thr180=) rs782560001 0.00004
NC_000012.12:g.121641295C>T rs781982396 0.00003
NC_000012.12:g.121641496C>T rs539371248 0.00003
NC_000012.12:g.121641076C>T rs782071653 0.00002
NC_000012.12:g.121641314C>T rs367886026 0.00002
NC_000012.12:g.121641454G>A rs782232018 0.00002
NC_000012.12:g.121641520G>A rs781878981 0.00002
NC_000012.12:g.121641568G>A rs370993629 0.00002
NC_000012.12:g.121641100C>T rs1893050404 0.00001
NC_000012.12:g.121641148G>A rs987522369 0.00001
NC_000012.12:g.121641187G>A rs782232478 0.00001
NC_000012.12:g.121641196C>T rs781980977 0.00001
NC_000012.12:g.121641199G>A rs1555324096 0.00001
NC_000012.12:g.121641298C>T rs782419547 0.00001
NC_000012.12:g.121641343C>A rs1160906886 0.00001
NC_000012.12:g.121641418C>T rs782091639 0.00001
NC_000012.12:g.121641619G>C rs1442961151 0.00001
NM_032790.3(ORAI1):c.309-18C>T rs781867634 0.00001
NC_000012.12:g.121641037G>T
NC_000012.12:g.121641070T>C
NC_000012.12:g.121641073C>T rs2136852459
NC_000012.12:g.121641088G>A
NC_000012.12:g.121641121A>C rs1555324082
NC_000012.12:g.121641181C>T rs782566002
NC_000012.12:g.121641193C>T
NC_000012.12:g.121641208C>G
NC_000012.12:g.121641214G>A rs547522547
NC_000012.12:g.121641253C>T
NC_000012.12:g.121641274C>T rs2136852852
NC_000012.12:g.121641286C>T rs1555324110
NC_000012.12:g.121641289G>T
NC_000012.12:g.121641367G>A rs1893056910
NC_000012.12:g.121641385C>G rs782238081
NC_000012.12:g.121641385C>T rs782238081
NC_000012.12:g.121641403C>G
NC_000012.12:g.121641436G>A rs2136853304
NC_000012.12:g.121641448C>T
NC_000012.12:g.121641475C>T rs782401288
NC_000012.12:g.121641490C>T
NC_000012.12:g.121641520G>C rs781878981
NC_000012.12:g.121641571G>A rs1893062288
NM_032790.4(ORAI1):c.306G>A (p.Val102=)
NM_032790.4(ORAI1):c.369C>T (p.Phe123=)
NM_032790.4(ORAI1):c.384A>G (p.Thr128=)
NM_032790.4(ORAI1):c.399G>A (p.Val133=)
NM_032790.4(ORAI1):c.408T>C (p.Phe136=)
NM_032790.4(ORAI1):c.426C>G (p.Thr142=)
NM_032790.4(ORAI1):c.492C>T (p.Pro164=)
NM_032790.4(ORAI1):c.552G>A (p.Thr184=) rs782215248
NM_032790.4(ORAI1):c.591C>T (p.Val197=)
NM_032790.4(ORAI1):c.657C>T (p.Gly219=)
NM_032790.4(ORAI1):c.750T>C (p.Phe250=)
NM_032790.4(ORAI1):c.762C>T (p.Ala254=)
NM_032790.4(ORAI1):c.807G>A (p.Gln269=)
NM_032790.4(ORAI1):c.888C>T (p.Pro296=) rs782446947

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