LPIN2

lipin 2

Summary

Mouse studies suggest that this gene functions during normal adipose tissue development and may play a role in human triglyceride metabolism. This gene represents a candidate gene for human lipodystrophy, characterized by loss of body fat, fatty liver, hypertriglyceridemia, and insulin resistance. [provided by RefSeq, Jul 2008]

Known Variants775 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs751266426	18:2,917,011	G/A	—	uncertain significance
rs767074158	18:2,917,074	T/C	—	uncertain significance
rs1164	18:2,917,152	C/T	—	benign
rs1985	18:2,917,223	T/A	—	benign
rs14916	18:2,917,276	A/G	—	benign
rs138807947	18:2,917,292	G/T	—	uncertain significance
rs4781	18:2,917,345	C/T	—	benign
rs7980	18:2,917,357	A/G	—	benign
rs202079191	18:2,917,368	G/A	—	benign
rs17880885	18:2,917,425	T/G	—	uncertain significance
rs886053741	18:2,917,461	G/A	—	uncertain significance
rs73375246	18:2,917,469	G/A	—	benign
rs886053742	18:2,917,504	G/C	—	uncertain significance
rs886053743	18:2,917,532	T/G	—	uncertain significance
rs886053744	18:2,917,567	T/C	—	uncertain significance
rs760097342	18:2,917,581	T/C	—	uncertain significance
rs559796642	18:2,917,686	C/T	—	uncertain significance
rs890590348	18:2,917,734	C/T	—	uncertain significance
rs149332969	18:2,917,738	C/T	—	likely benign
rs8091401	18:2,917,798	G/C	—	benign
rs760089028	18:2,917,874	G/A	—	uncertain significance
rs553336397	18:2,917,879	G/A	—	uncertain significance
rs536036852	18:2,917,900	C/T	—	uncertain significance
rs555969171	18:2,917,901	G/A	—	likely benign
rs16944033	18:2,918,050	A/G	—	benign
rs886053746	18:2,918,075	G/T	—	uncertain significance
rs561577089	18:2,918,188	C/T	—	likely benign
rs112529707	18:2,918,215	G/T	—	likely benign
rs75771450	18:2,918,417	G/C	—	uncertain significance
rs886053747	18:2,918,464	C/T	—	uncertain significance
rs886740636	18:2,918,481	T/C	—	uncertain significance
rs551448975	18:2,918,549	T/C	—	uncertain significance
rs112588494	18:2,918,600	T/C	—	benign
rs111366726	18:2,918,669	A/G	—	benign
rs144299426	18:2,918,705	C/T	—	likely benign
rs886053748	18:2,918,732	T/C	—	uncertain significance
rs544570644	18:2,918,777	C/G	—	uncertain significance
rs751740607	18:2,918,787	A/G	—	uncertain significance
rs113346639	18:2,918,789	C/T	—	benign
rs1321388898	18:2,918,794	G/A	—	uncertain significance
rs577975091	18:2,918,797	C/T	—	uncertain significance
rs540306659	18:2,918,818	A/C	—	uncertain significance
rs560770304	18:2,918,829	T/C	—	uncertain significance
rs532711041	18:2,918,848	C/T	—	uncertain significance
rs552844041	18:2,918,873	C/T	—	uncertain significance
rs745743898	18:2,918,874	G/A	—	uncertain significance
rs1257894281	18:2,919,052	G/A	—	uncertain significance
rs886053749	18:2,919,071	C/T	—	uncertain significance
rs566472161	18:2,919,092	C/T	—	uncertain significance
rs147362027	18:2,919,112	C/T	—	likely benign
rs1240536600	18:2,919,134	A/G	—	uncertain significance
rs139015163	18:2,919,144	T/C	—	likely benign
rs1384648245	18:2,919,145	A/G	—	uncertain significance
rs886053750	18:2,919,165	C/T	—	uncertain significance
rs913148654	18:2,919,187	G/A	—	uncertain significance
rs149858117	18:2,919,209	C/T	—	benign
rs563088438	18:2,919,214	G/C	—	likely benign
rs59566682	18:2,919,239	G/A	—	benign
rs551503883	18:2,919,264	C/T	—	uncertain significance
rs529650414	18:2,919,265	G/A	—	uncertain significance
rs886053751	18:2,919,270	C/T	—	uncertain significance
rs546238775	18:2,919,307	A/G	—	uncertain significance
rs3810065	18:2,919,341	T/G	—	benign
rs112444822	18:2,919,346	C/T	—	uncertain significance
rs1032890815	18:2,919,357	C/G	—	uncertain significance
rs78462116	18:2,919,388	A/T	—	uncertain significance
rs886053752	18:2,919,394	A/C	—	uncertain significance
rs2077017832	18:2,919,436	T/C	—	uncertain significance
rs73375250	18:2,919,441	C/T	—	likely benign
rs886053753	18:2,919,457	C/T	—	uncertain significance
rs540627141	18:2,919,458	C/T	—	uncertain significance
rs776259595	18:2,919,463	A/C	—	uncertain significance
rs747730329	18:2,919,468	C/T	—	uncertain significance
rs547125074	18:2,919,478	T/G	—	uncertain significance
rs769197357	18:2,919,481	C/T	—	uncertain significance
rs144349249	18:2,919,485	G/A	—	uncertain significance
rs146605124	18:2,919,486	G/C	—	uncertain significance
rs1294529732	18:2,919,487	C/T	—	uncertain significance
rs3810064	18:2,919,494	A/C	—	benign
rs567530586	18:2,919,495	A/G	—	uncertain significance
rs542453339	18:2,919,499	C/G	—	uncertain significance
rs924335721	18:2,919,513	G/A	—	uncertain significance
rs190290283	18:2,919,518	G/A	—	uncertain significance
rs948592383	18:2,919,519	C/T	—	uncertain significance
rs886053754	18:2,919,524	T/C	—	uncertain significance
rs886053755	18:2,919,566	C/T	—	uncertain significance
rs76325993	18:2,919,568	T/C	—	benign
rs145046223	18:2,919,592	T/C	—	benign
rs607549	18:2,919,606	T/A	—	benign
rs186189096	18:2,919,625	G/A	—	uncertain significance
rs754769201	18:2,919,631	T/C	—	uncertain significance
rs16944040	18:2,919,634	T/G	—	benign
rs118142692	18:2,919,654	C/T	—	benign
rs112795993	18:2,919,734	T/C	—	benign
rs576721761	18:2,919,771	A/G	—	uncertain significance
rs760055818	18:2,919,774	C/T	—	uncertain significance
rs886053756	18:2,919,784	A/G	—	uncertain significance
rs886053757	18:2,919,785	G/A	—	uncertain significance
rs35176958	18:2,919,790	A/G	—	likely benign
rs886053758	18:2,919,798	C/T	—	uncertain significance

Showing 100 of 775 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.