ClinVar Miner

List of variants in gene AMN reported as benign for abdominal and pelvic region disorder

Included ClinVar conditions (1042):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP
NM_030943.3(AMN):c.1170-37C>G rs148815688
NM_030943.3(AMN):c.1170-6C>T rs386834164
NM_030943.3(AMN):c.165G>A (p.Met55Ile) rs61731158
NM_030943.3(AMN):c.296-9C>T rs373204347
NM_030943.3(AMN):c.363G>A (p.Gly121=) rs141455061
NM_030943.3(AMN):c.829A>G (p.Thr277Ala) rs146499374
NM_030943.4(AMN):c.208-10T>C rs115851517
NM_030943.4(AMN):c.321T>C (p.Ser107=) rs563004567
NM_030943.4(AMN):c.324C>T (p.Asp108=) rs7140429
NM_030943.4(AMN):c.909C>T (p.Ala303=) rs373382273
NM_030943.4(AMN):c.93C>T (p.Asp31=) rs772599857

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