ClinVar Miner

List of variants in gene INF2 reported as benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
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HGVS dbSNP
NM_022489.4(INF2):c.*437G>A rs1128866
NM_022489.4(INF2):c.*536G>T rs1128880
NM_022489.4(INF2):c.-10G>A rs115602636
NM_022489.4(INF2):c.-85G>A rs141884370
NM_022489.4(INF2):c.105C>T (p.Pro35=) rs4983530
NM_022489.4(INF2):c.1227G>T (p.Ser409=) rs3809455
NM_022489.4(INF2):c.2310+8del rs3840006
NM_022489.4(INF2):c.2322C>T (p.Thr774=) rs59751492
NM_022489.4(INF2):c.2571C>T (p.Ser857=) rs62640005
NM_022489.4(INF2):c.2640T>C (p.Asp880=) rs10133301
NM_022489.4(INF2):c.2775+15C>T rs73347508
NM_022489.4(INF2):c.3066T>C (p.Asp1022=) rs4983535
NM_022489.4(INF2):c.3153C>T (p.Asp1051=) rs117457867
NM_022489.4(INF2):c.3207A>C (p.Pro1069=) rs1128840
NM_022489.4(INF2):c.3207A>G (p.Pro1069=) rs1128840
NM_022489.4(INF2):c.3286C>T (p.Pro1096Ser) rs34251364
NM_022489.4(INF2):c.3478G>A (p.Gly1160Ser) rs9672065
NM_022489.4(INF2):c.391+6C>T rs75115369
NM_022489.4(INF2):c.42G>A (p.Leu14=) rs62638758

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