List of variants in gene INF2 reported as benign by Athena Diagnostics Inc

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

Total variants: 23

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HGVS	dbSNP	gnomAD frequency
NM_022489.4(INF2):c.105C>T (p.Pro35=)	rs4983530	0.98049
NM_022489.4(INF2):c.2640T>C (p.Asp880=)	rs10133301	0.88426
NM_022489.4(INF2):c.3066T>C (p.Asp1022=)	rs4983535	0.79980
NM_022489.4(INF2):c.2310+8del	rs3840006	0.58720
NM_022489.4(INF2):c.3286C>T (p.Pro1096Ser)	rs34251364	0.05864
NM_022489.4(INF2):c.2322C>T (p.Thr774=)	rs59751492	0.02373
NM_022489.4(INF2):c.3478G>A (p.Gly1160Ser)	rs9672065	0.01930
NM_022489.4(INF2):c.2571C>T (p.Ser857=)	rs62640005	0.01396
NM_022489.4(INF2):c.42G>A (p.Leu14=)	rs62638758	0.01192
NM_022489.4(INF2):c.3153C>T (p.Asp1051=)	rs117457867	0.01185
NM_022489.4(INF2):c.2630G>A (p.Arg877Gln)	rs142678449	0.00781
NM_022489.4(INF2):c.879G>A (p.Ser293=)	rs184709736	0.00543
NM_022489.4(INF2):c.3108T>C (p.Leu1036=)	rs186075307	0.00532
NM_022489.4(INF2):c.558C>T (p.Ser186=)	rs150714865	0.00158
NM_022489.4(INF2):c.264C>T (p.Gly88=)	rs201587219	0.00150
NM_022489.4(INF2):c.3612G>A (p.Ser1204=)	rs150811244	0.00134
NM_022489.4(INF2):c.1950-10C>T	rs199987321	0.00082
NM_022489.4(INF2):c.639G>A (p.Ala213=)	rs149858291	0.00031
NM_022489.4(INF2):c.1755G>A (p.Ala585=)	rs375573206	0.00013
NM_022489.4(INF2):c.1582C>T (p.Pro528Ser)	rs181694819
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.391+6C>T	rs75115369

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