ClinVar Miner

List of variants studied for allergic disease

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_181078.3(IL21R):c.-17+563G>A rs117535117 0.00901
NM_181078.3(IL21R):c.824G>A (p.Arg275Gln) rs52822694 0.00673
NM_000418.4(IL4R):c.1160C>T (p.Ser387Leu) rs6413500 0.00374
NM_181078.3(IL21R):c.1033G>A (p.Gly345Ser) rs56148525 0.00271
NM_000418.4(IL4R):c.1774G>T (p.Val592Leu) rs138392496 0.00156
NM_181078.3(IL21R):c.605C>T (p.Ala202Val) rs147673485 0.00055
NM_181078.3(IL21R):c.1550G>A (p.Arg517Gln) rs761950657 0.00007
NM_181078.3(IL21R):c.995C>T (p.Thr332Met) rs761814669 0.00007
46;XX;t(4;14)(p15.2;q13)dn
GRCh37/hg19 6p24.1-23(chr6:12536624-13968949)
HAVCR1, 6-AA INS
NM_000418.4(IL4R):c.134A>G (p.Glu45Gly)
NM_001379110.1(SLC9A6):c.1190C>A (p.Ala397Glu) rs1556619324
NM_002016.2(FLG):c.1501C>T (p.Arg501Ter) rs61816761
NM_002016.2(FLG):c.2282_2285del (p.Ser761fs) rs558269137

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