ClinVar Miner

List of variants in gene LPIN2 reported as likely benign for anemia (disease)

Included ClinVar conditions (281):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 51
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HGVS dbSNP
NM_014646.2(LPIN2):c.*1077C>G rs563088438
NM_014646.2(LPIN2):c.*1147A>G
NM_014646.2(LPIN2):c.*1179G>A rs147362027
NM_014646.2(LPIN2):c.*151G>A rs571000282
NM_014646.2(LPIN2):c.*1586G>A rs144299426
NM_014646.2(LPIN2):c.*158G>A rs547872442
NM_014646.2(LPIN2):c.*2076C>A rs112529707
NM_014646.2(LPIN2):c.*2103G>A rs561577089
NM_014646.2(LPIN2):c.*2197_*2198del rs55834965
NM_014646.2(LPIN2):c.*2390C>T rs555969171
NM_014646.2(LPIN2):c.*2553G>A
NM_014646.2(LPIN2):c.*2924del rs148191039
NM_014646.2(LPIN2):c.*358G>A rs184193388
NM_014646.2(LPIN2):c.*850G>A
NM_014646.2(LPIN2):c.-66C>T rs116643915
NM_014646.2(LPIN2):c.1026G>T (p.Val342=) rs1232642116
NM_014646.2(LPIN2):c.1043C>T (p.Pro348Leu) rs34676691
NM_014646.2(LPIN2):c.1122A>G (p.Ser374=) rs748347465
NM_014646.2(LPIN2):c.1159A>G (p.Lys387Glu) rs104895501
NM_014646.2(LPIN2):c.1169-7del rs746626720
NM_014646.2(LPIN2):c.1275G>A (p.Ser425=) rs1051720856
NM_014646.2(LPIN2):c.1329C>A (p.Ser443=) rs759651506
NM_014646.2(LPIN2):c.1489G>A (p.Glu497Lys) rs201325845
NM_014646.2(LPIN2):c.1510C>T (p.Leu504Phe) rs104895500
NM_014646.2(LPIN2):c.1735T>C (p.Ser579Pro) rs150022314
NM_014646.2(LPIN2):c.1797G>A (p.Pro599=) rs772568696
NM_014646.2(LPIN2):c.1800C>T (p.Ala600=) rs369572309
NM_014646.2(LPIN2):c.1801G>A (p.Glu601Lys) rs61735393
NM_014646.2(LPIN2):c.1939-14T>C rs370284164
NM_014646.2(LPIN2):c.1939-2del rs745529823
NM_014646.2(LPIN2):c.2088-10G>A rs374043211
NM_014646.2(LPIN2):c.2088-7T>G rs199713353
NM_014646.2(LPIN2):c.2316C>A (p.Ser772=) rs145270447
NM_014646.2(LPIN2):c.2316C>T (p.Ser772=) rs145270447
NM_014646.2(LPIN2):c.2371C>T (p.Leu791=) rs373520277
NM_014646.2(LPIN2):c.2443-9C>T rs191749331
NM_014646.2(LPIN2):c.2445T>C (p.Asp815=) rs140249737
NM_014646.2(LPIN2):c.2535A>C (p.Gly845=) rs186864136
NM_014646.2(LPIN2):c.2568C>T (p.Leu856=) rs149862905
NM_014646.2(LPIN2):c.2583C>T (p.Phe861=) rs141043192
NM_014646.2(LPIN2):c.2610C>T (p.Ser870=) rs145412418
NM_014646.2(LPIN2):c.2621G>T (p.Cys874Phe) rs201160155
NM_014646.2(LPIN2):c.2625G>A (p.Pro875=) rs187572602
NM_014646.2(LPIN2):c.2671G>A (p.Asp891Asn) rs200648652
NM_014646.2(LPIN2):c.446C>T (p.Pro149Leu) rs147615538
NM_014646.2(LPIN2):c.516C>T (p.Ala172=) rs150312425
NM_014646.2(LPIN2):c.608C>T (p.Ser203Phe) rs144555528
NM_014646.2(LPIN2):c.756G>A (p.Ala252=) rs570485374
NM_014646.2(LPIN2):c.840A>G (p.Arg280=) rs780138552
NM_014646.2(LPIN2):c.87G>A (p.Gly29=) rs1346313879
NM_014646.2(LPIN2):c.991G>T (p.Ala331Ser) rs80338805

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