ClinVar Miner

List of variants in gene CLDN19 studied for abdominal and pelvic region disorder

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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HGVS dbSNP
NM_148960.3(CLDN19):c.169C>G (p.Gln57Glu) rs118203980
NM_148960.3(CLDN19):c.169C>T (p.Gln57Ter) rs118203980
NM_148960.3(CLDN19):c.269T>C (p.Leu90Pro) rs118203981
NM_148960.3(CLDN19):c.269T>G (p.Leu90Arg) rs118203981
NM_148960.3(CLDN19):c.388G>T (p.Gly130Cys) rs1557551678
NM_148960.3(CLDN19):c.535G>A (p.Gly179Ser) rs145591298
NM_148960.3(CLDN19):c.59G>A (p.Gly20Asp) rs118203979

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