ClinVar Miner

List of variants in gene LPIN1 reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_001349206.2(LPIN1):c.*624A>G rs2716639 0.81419
NM_001349206.2(LPIN1):c.*1400T>C rs11524 0.21720
NM_001349206.2(LPIN1):c.*897C>T rs1050800 0.12057
NM_001349206.2(LPIN1):c.552C>T (p.Ile184=) rs11538448 0.09460
NM_001349206.2(LPIN1):c.657G>A (p.Leu219=) rs59909741 0.06723
NM_001349206.2(LPIN1):c.*2086C>G rs77333662 0.06326
NM_001349206.2(LPIN1):c.*425G>A rs74564998 0.06315
NM_001349206.2(LPIN1):c.*1570C>G rs10700 0.06283
NM_001349206.2(LPIN1):c.2358G>C (p.Gly786=) rs61732581 0.04121
NM_001349206.2(LPIN1):c.1936C>T (p.Pro646Ser) rs4669781 0.03693
NM_001349206.2(LPIN1):c.1588G>A (p.Val530Met) rs33997857 0.01739
NM_001349206.2(LPIN1):c.*1699G>A rs113103707 0.01727
NM_001349206.2(LPIN1):c.*2491G>A rs139423804 0.01368
NM_001349206.2(LPIN1):c.*326C>T rs73917820 0.01235
NM_001349206.2(LPIN1):c.420C>T (p.Ile140=) rs75945731 0.01127
NM_001349206.2(LPIN1):c.*623A>C rs76762966 0.00990
NM_001349206.2(LPIN1):c.696G>C (p.Ser232=) rs145180224 0.00818
NM_001349206.2(LPIN1):c.*2302G>T rs116614346 0.00727
NM_001349206.2(LPIN1):c.*682G>C rs183367696 0.00193
NM_001349206.2(LPIN1):c.*1671C>T rs187684475 0.00126

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