Variants in gene LPIN2 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 27

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HGVS	dbSNP	gnomAD frequency
NM_001375808.2(LPIN2):c.1510C>T (p.Leu504Phe)	rs104895500	0.00253
NM_001375808.2(LPIN2):c.-10+1381T>C	rs566304730	0.00176
NM_001375808.2(LPIN2):c.991G>T (p.Ala331Ser)	rs80338805	0.00142
NM_001375808.2(LPIN2):c.2443-9C>T	rs191749331	0.00047
NM_001375808.2(LPIN2):c.2568C>T (p.Leu856=)	rs149862905	0.00045
NM_001375808.2(LPIN2):c.446C>T (p.Pro149Leu)	rs147615538	0.00038
NM_001375808.2(LPIN2):c.2671G>A (p.Asp891Asn)	rs200648652	0.00034
NM_001375808.2(LPIN2):c.2625G>A (p.Pro875=)	rs187572602	0.00025
NM_001375808.2(LPIN2):c.1168+6C>T	rs200130790	0.00024
NM_001375808.2(LPIN2):c.2445T>C (p.Asp815=)	rs140249737	0.00021
NM_001375808.2(LPIN2):c.1132C>T (p.Pro378Ser)	rs201678207	0.00018
NM_001375808.2(LPIN2):c.2327+10C>T	rs367921036	0.00018
NM_001375808.2(LPIN2):c.2328-13A>T	rs199830303	0.00017
NM_001375808.2(LPIN2):c.2535A>C (p.Gly845=)	rs186864136	0.00012
NM_001375808.2(LPIN2):c.1169-3C>T	rs200259086	0.00011
NM_001375808.2(LPIN2):c.1395C>T (p.Asp465=)	rs143562359	0.00008
NM_001375808.2(LPIN2):c.1888G>A (p.Gly630Ser)	rs148607670	0.00006
NM_001375808.2(LPIN2):c.1347C>T (p.Ser449=)	rs773074044	0.00002
NM_001375808.2(LPIN2):c.1404C>T (p.Asp468=)	rs376147435	0.00001
NM_001375808.2(LPIN2):c.54C>A (p.Leu18=)	rs753729438	0.00001
NM_001375808.2(LPIN2):c.590+8T>G	rs760846327	0.00001
NM_001375808.2(LPIN2):c.756G>A (p.Ala252=)	rs570485374	0.00001
NM_001375808.2(LPIN2):c.1169-7del	rs746626720
NM_001375808.2(LPIN2):c.1716A>G (p.Pro572=)	rs2077138820
NM_001375808.2(LPIN2):c.1939-2del	rs745529823
NM_001375808.2(LPIN2):c.2211C>T (p.Ala737=)	rs886053765
NM_001375808.2(LPIN2):c.2621G>T (p.Cys874Phe)	rs201160155

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