ClinVar Miner

List of variants studied for Behcet disease

Included ClinVar conditions (1):
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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_001145306.2(CDK6):c.647+21377A>G rs2282983 0.43846
NM_003855.5(IL18R1):c.59-1038C>A rs4851569 0.33141
NM_003855.5(IL18R1):c.-29+1269C>T rs12999364 0.31121
NM_003855.5(IL18R1):c.-29+2476T>G rs12987977 0.31111
NM_001145306.2(CDK6):c.*5310T>C rs42034 0.19453
NM_001282225.2(ADA2):c.1045G>A (p.Val349Ile) rs74317375 0.00227
NM_001282225.2(ADA2):c.927G>A (p.Met309Ile) rs146597836 0.00156
NM_001065.4(TNFRSF1A):c.935G>A (p.Arg312Lys) rs200900510 0.00113
NM_022162.2(NOD2):c.241C>G (p.Leu81Val) rs34936594 0.00046
NM_003978.5(PSTPIP1):c.203C>T (p.Thr68Met) rs201872851 0.00041
NM_001282225.2(ADA2):c.145C>T (p.Arg49Trp) rs199614299 0.00013
NM_001065.4(TNFRSF1A):c.596T>C (p.Ile199Thr) rs104895247 0.00011
NM_001282225.2(ADA2):c.740C>T (p.Ala247Val) rs750868279 0.00005
NM_000243.3(MEFV):c.1099C>G (p.Leu367Val) rs1057519328 0.00002
NM_000243.3(MEFV):c.1211A>G (p.His404Arg) rs755659290 0.00001
NM_003978.5(PSTPIP1):c.364G>A (p.Val122Ile) rs886041107 0.00001
NM_000243.3(MEFV):c.332G>A (p.Gly111Glu) rs751454741
NM_001065.3(TNFRSF1A):c.463C>T (p.His155Tyr) rs886039866
NM_001370466.1(NOD2):c.964C>T (p.Leu322Phe) rs752615209
NM_003978.5(PSTPIP1):c.865G>C (p.Asp289His) rs774164456
NM_022162.2(NOD2):c.2197G>T (p.Val733Leu) rs746055479
NM_022162.2(NOD2):c.2446G>A rs886040969

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