ClinVar Miner

List of variants reported as protective by OMIM

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Total variants: 78
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HGVS dbSNP
CCL11, -1385G-A
CCL2, -2136A-T
CCL2, 767C-G
CD209, -336A-G
CR1, 3650A-G
CX3CR1:c.[841G>A;935C>T] (p.Val294Ile;Thr280Met)
CYP2A6*4A
EDNRA, -231G
GABABR2, HAPLOTYPE, CACA (rs1435252, rs3780422, rs2779562, rs3750344)
IFNG, +874A-T
IFNGR1, -56C-T
MC4R, VAL103ILE (rs2229616)
MPO, -463G-A
MUC7, 69-BP DUP, VARIABLE REPEATS
NM_000063.6(C2):c.1360+62G>T rs547154
NM_000129.3(F13A1):c.103G>T (p.Val35Leu) rs5985
NM_000133.3(F9):c.580A>G (p.Thr194Ala) rs6048
NM_000253.3(MTTP):c.383T>C (p.Ile128Thr) rs3816873
NM_000311.5(PRNP):c.380G>T (p.Gly127Val) rs267606980
NM_000342.4(SLC4A1):c.1199_1225del (p.Ala400_Ala408del) rs769664228
NM_000418.4(IL4R):c.1507T>C (p.Ser503Pro) rs1805015
NM_000418.4(IL4R):c.223A>G (p.Ile75Val) rs1805010
NM_000484.4(APP):c.2017G>A (p.Ala673Thr) rs63750847
NM_000518.4(HBB):c.19G>A (p.Glu7Lys) rs33930165
NM_000518.5(HBB):c.20A>T (p.Glu7Val) rs334
NM_000518.5(HBB):c.79G>A (p.Glu27Lys) rs33950507
NM_000579.3(CCR5):c.-301+246A>G rs1799987
NM_000579.3(CCR5):c.180G>T (p.Arg60Ser) rs1800940
NM_000579.3(CCR5):c.303T>A (p.Cys101Ter) rs1800560
NM_000579.3(CCR5):c.554_585del (p.Ser185fs) rs333
NM_000609.7(CXCL12):c.266+535G>A rs387906400
NM_000668.5(ADH1B):c.143A= (p.His48=) rs1229984
NM_000668.6(ADH1B):c.1108C>T (p.Arg370Cys) rs2066702
NM_000669.5(ADH1C):c.1048A>G (p.Ile350Val) rs698
NM_000669.5(ADH1C):c.815G>A (p.Arg272Gln) rs1693482
NM_000690.4(ALDH2):c.1510G>A (p.Glu504Lys) rs671
NM_000744.6(CHRNA4):c.1629C>T (p.Ser543=) rs1044396
NM_000744.6(CHRNA4):c.1659G>A (p.Ala553=) rs1044397
NM_000875.5(IGF1R):c.119G>T (p.Arg40Leu) rs1409058783
NM_000875.5(IGF1R):c.1532G>A (p.Arg511Gln) rs33958176
NM_000875.5(IGF1R):c.2201G>T (p.Arg734Ile) rs1555460945
NM_000875.5(IGF1R):c.2216G>A (p.Arg739Gln) rs121912429
NM_000875.5(IGF1R):c.265C>T (p.Arg89Ter) rs121912428
NM_000875.5(IGF1R):c.361G>A (p.Glu121Lys) rs1555434208
NM_000875.5(IGF1R):c.413G>A (p.Arg138Gln) rs121912426
NM_000875.5(IGF1R):c.435A>C (p.Lys145Asn) rs121912427
NM_000875.5(IGF1R):c.700G>A (p.Glu234Lys) rs1253103806
NM_001001547.2(CD36):c.120+399TG[12]
NM_001039661.1(TIRAP):c.539C>T (p.Ser180Leu) rs8177374
NM_001067.4(TOP2A):c.1460G>A (p.Arg487Lys) rs267607133
NM_001123041.2(CCR2):c.190G>A (p.Val64Ile) rs1799864
NM_001172560.1(SSTR5):c.718C>T (p.Arg240Trp) rs121917877
NM_001172813.2(SLC30A8):c.-47_-41del rs587777582
NM_001172813.2(SLC30A8):c.265C>T (p.Arg89Ter) rs200185429
NM_001228.4(CASP8):c.-937_-932del rs3834129
NM_001228.4(CASP8):c.904G>C (p.Asp302His) rs1045485
NM_001710.5(CFB):c.95G>A (p.Arg32Gln) rs641153
NM_002036.3(ACKR1):c.-67T>C rs2814778
NM_002101.4(GYPC):c.107_190del (p.Glu36_Ala63del) rs1553470034
NM_002312.3(LIG4):c.26C>T (p.Thr9Ile) rs1805388
NM_002312.3(LIG4):c.8C>T (p.Ala3Val) rs1805389
NM_002539.3(ODC1):c.-128+109G>A rs2302615
NM_002770.4(PRSS2):c.571G>A (p.Gly191Arg) rs61734659
NM_003263.4(TLR1):c.1805G>T (p.Ser602Ile) rs5743618
NM_003265.2(TLR3):c.1234C>T (p.Leu412Phe) rs3775291
NM_003268.6(TLR5):c.1174C>T (p.Arg392Ter) rs5744168
NM_004001.4(FCGR2B):c.695T>C (p.Ile232Thr) rs1050501
NM_004137.4(KCNMB1):c.193G>A (p.Glu65Lys) rs11739136
NM_005228.5(EGFR):c.2369C>T (p.Thr790Met) rs121434569
NM_020975.6(RET):c.*1969T>C rs3026785
NM_138694.4(PKHD1):c.107C>T (p.Thr36Met) rs137852944
NM_144701.3(IL23R):c.1142G>A (p.Arg381Gln) rs11209026
NM_153758.3(IL19):c.-35+1984T>G rs1800872
NOS2A, -1173C-T
NOS2A, -969G-C
SLC6A3*9
TNF, -863C-A
m.10398A>G rs2853826

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