List of variants reported as benign for Majeed syndrome by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 36

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HGVS	dbSNP	gnomAD frequency
NM_001375808.2(LPIN2):c.*685T>A	rs607549	0.71526
NM_001375808.2(LPIN2):c.*2934C>T	rs7980	0.50276
NM_001375808.2(LPIN2):c.*3C>T	rs3745012	0.26634
NM_001375808.2(LPIN2):c.*3068A>T	rs1985	0.24248
NM_001375808.2(LPIN2):c.*3139A>G	rs1164	0.18839
NM_001375808.2(LPIN2):c.*657A>C	rs16944040	0.16453
NM_001375808.2(LPIN2):c.*2493C>G	rs8091401	0.08828
NM_001375808.2(LPIN2):c.*1052T>C	rs59566682	0.06708
NM_001375808.2(LPIN2):c.*501T>C	rs35176958	0.05856
NM_001375808.2(LPIN2):c.*2923C>T	rs202079191	0.04421
NM_001375808.2(LPIN2):c.*2946G>A	rs4781	0.03480
NM_001375808.2(LPIN2):c.*557G>A	rs112795993	0.03331
NM_001375808.2(LPIN2):c.-10+1342C>G	rs59096963	0.03286
NM_001375808.2(LPIN2):c.-10+1343C>G	rs58940048	0.03285
NM_001375808.2(LPIN2):c.*2241T>C	rs16944033	0.03080
NM_001375808.2(LPIN2):c.1168+11G>C	rs79439091	0.02576
NM_001375808.2(LPIN2):c.*950A>C	rs3810065	0.01773
NM_001375808.2(LPIN2):c.*1502G>A	rs113346639	0.01434
NM_001375808.2(LPIN2):c.*99C>T	rs143728428	0.01403
NM_001375808.2(LPIN2):c.2223C>T (p.Ala741=)	rs17555442	0.01175
NM_001375808.2(LPIN2):c.*2822C>T	rs73375246	0.00916
NM_001375808.2(LPIN2):c.*1691A>G	rs112588494	0.00863
NM_001375808.2(LPIN2):c.-10+1313C>T	rs116643915	0.00793
NM_001375808.2(LPIN2):c.147C>T (p.His49=)	rs17886056	0.00707
NM_001375808.2(LPIN2):c.*3015T>C	rs14916	0.00541
NM_001375808.2(LPIN2):c.*1622T>C	rs111366726	0.00538
NM_001375808.2(LPIN2):c.*1082G>A	rs149858117	0.00508
NM_001375808.2(LPIN2):c.590+6A>G	rs73375280	0.00505
NM_001375808.2(LPIN2):c.*797T>G	rs3810064	0.00180
NM_001375808.2(LPIN2):c.991G>T (p.Ala331Ser)	rs80338805	0.00142
NM_001375808.2(LPIN2):c.*699A>G	rs145046223	0.00092
NM_001375808.2(LPIN2):c.1876C>T (p.Pro626Ser)	rs150806357	0.00083
NM_001375808.2(LPIN2):c.*637G>A	rs118142692	0.00058
NM_001375808.2(LPIN2):c.608C>T (p.Ser203Phe)	rs144555528	0.00006
NM_001375808.2(LPIN2):c.*723A>G	rs76325993
NM_001375808.2(LPIN2):c.*947dup	rs3840906

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