ClinVar Miner

List of variants in gene combination SP110, SP140 reported as benign for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP
NM_080424.2(SP110):c.334C>T (p.Arg112Trp) rs1129411
NM_080424.2(SP110):c.376G>A (p.Gly126Ser) rs41309088
NM_080424.2(SP110):c.383C>T (p.Ala128Val) rs11556887
NM_080424.2(SP110):c.522C>T (p.Pro174=) rs144428054
NM_080424.2(SP110):c.583+8A>G rs114743173
NM_080424.2(SP110):c.584-10C>G rs148591984
NM_080424.2(SP110):c.584-9C>T rs41309096
NM_080424.2(SP110):c.617C>T (p.Ala206Val) rs28930679
NM_080424.2(SP110):c.619G>A (p.Glu207Lys) rs9061
NM_080424.2(SP110):c.895G>A (p.Gly299Arg) rs1365776

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