ClinVar Miner

List of variants in gene SLC34A1 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (961):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP
NM_003052.5(SLC34A1):c.*196C>T
NM_003052.5(SLC34A1):c.*212G>T
NM_003052.5(SLC34A1):c.*239C>A rs768911630
NM_003052.5(SLC34A1):c.*241C>T
NM_003052.5(SLC34A1):c.*301T>C
NM_003052.5(SLC34A1):c.*323G>A rs886060469
NM_003052.5(SLC34A1):c.*331A>G
NM_003052.5(SLC34A1):c.*392A>G rs886060470
NM_003052.5(SLC34A1):c.*406C>T
NM_003052.5(SLC34A1):c.*505C>T
NM_003052.5(SLC34A1):c.*52C>T
NM_003052.5(SLC34A1):c.*60G>A rs886060467
NM_003052.5(SLC34A1):c.*65G>A
NM_003052.5(SLC34A1):c.*79G>C rs886060468
NM_003052.5(SLC34A1):c.-48G>C rs886060466
NM_003052.5(SLC34A1):c.-68G>A rs774774202
NM_003052.5(SLC34A1):c.1006+1G>A rs200095793
NM_003052.5(SLC34A1):c.110-6C>T rs773115741
NM_003052.5(SLC34A1):c.1466A>G (p.Tyr489Cys)
NM_003052.5(SLC34A1):c.1708C>A (p.Pro570Thr)
NM_003052.5(SLC34A1):c.315A>C (p.Pro105=)
NM_003052.5(SLC34A1):c.94G>A (p.Val32Met)

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