ClinVar Miner

List of variants in gene GSS reported as likely benign for immune system disorder

Included ClinVar conditions (908):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 198
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HGVS dbSNP gnomAD frequency
NM_000178.4(GSS):c.-63G>C rs192442930 0.00445
NM_000178.4(GSS):c.768-3C>T rs184506175 0.00189
NM_000178.4(GSS):c.973C>T (p.Pro325Ser) rs11905938 0.00171
NM_000178.4(GSS):c.988C>T (p.Arg330Cys) rs148640446 0.00138
NM_000178.4(GSS):c.1253G>A (p.Arg418Gln) rs150141794 0.00084
NM_000178.4(GSS):c.1158G>A (p.Leu386=) rs141866304 0.00073
NM_000178.4(GSS):c.491+18C>G rs200511586 0.00065
NM_000178.4(GSS):c.468C>T (p.Ala156=) rs79420079 0.00036
NM_000178.4(GSS):c.768-7G>A rs371625892 0.00026
NM_000178.4(GSS):c.707G>A (p.Arg236Gln) rs34239729 0.00021
NM_000178.4(GSS):c.1301+14G>C rs200219120 0.00019
NM_000178.4(GSS):c.399C>T (p.Ser133=) rs181055807 0.00016
NM_000178.4(GSS):c.246C>T (p.Asn82=) rs375957984 0.00014
NM_000178.4(GSS):c.1126G>A (p.Gly376Arg) rs146267300 0.00007
NM_000178.4(GSS):c.1362C>T (p.Ile454=) rs911134339 0.00003
NM_000178.4(GSS):c.1056C>T (p.Ala352=) rs142345902 0.00002
NM_000178.4(GSS):c.1239T>C (p.Pro413=) rs201406090 0.00002
NM_000178.4(GSS):c.1047G>A (p.Gln349=) rs772123367 0.00001
NM_000178.4(GSS):c.126G>A (p.Ser42=) rs200259388 0.00001
NM_000178.4(GSS):c.204G>T (p.Val68=) rs2081519190 0.00001
NM_000178.4(GSS):c.300C>T (p.Thr100=) rs781170028 0.00001
NM_000178.4(GSS):c.981T>C (p.Ala327=) rs761196398 0.00001
NM_000178.4(GSS):c.*69G>T rs200882573
NM_000178.4(GSS):c.1011C>T (p.Gly337=)
NM_000178.4(GSS):c.1029+10C>A
NM_000178.4(GSS):c.1029+11A>G
NM_000178.4(GSS):c.1029+13C>T
NM_000178.4(GSS):c.1029+14C>T
NM_000178.4(GSS):c.1029+14del
NM_000178.4(GSS):c.1030-10C>T
NM_000178.4(GSS):c.1030-12G>T
NM_000178.4(GSS):c.1030-14C>T
NM_000178.4(GSS):c.1030-15T>G
NM_000178.4(GSS):c.1030-16T>G
NM_000178.4(GSS):c.1030-19G>A
NM_000178.4(GSS):c.1050C>T (p.Ala350=)
NM_000178.4(GSS):c.1053C>T (p.Ile351=)
NM_000178.4(GSS):c.1059G>A (p.Glu353=)
NM_000178.4(GSS):c.105C>G (p.Thr35=) rs1236802847
NM_000178.4(GSS):c.1065T>A (p.Leu355=)
NM_000178.4(GSS):c.1080G>A (p.Arg360=)
NM_000178.4(GSS):c.108A>G (p.Ser36=)
NM_000178.4(GSS):c.1095C>T (p.Pro365=)
NM_000178.4(GSS):c.1111+14C>T
NM_000178.4(GSS):c.1111+16T>C
NM_000178.4(GSS):c.1111+8G>T
NM_000178.4(GSS):c.1112-18T>A
NM_000178.4(GSS):c.1112-18T>C
NM_000178.4(GSS):c.1112-4G>A
NM_000178.4(GSS):c.111G>A (p.Gln37=)
NM_000178.4(GSS):c.1120C>T (p.Leu374=)
NM_000178.4(GSS):c.1122A>G (p.Leu374=)
NM_000178.4(GSS):c.1134A>G (p.Glu378=)
NM_000178.4(GSS):c.1156C>T (p.Leu386=)
NM_000178.4(GSS):c.1167T>C (p.Ser389=)
NM_000178.4(GSS):c.1182C>T (p.Ser394=)
NM_000178.4(GSS):c.1203C>A (p.Ile401=)
NM_000178.4(GSS):c.1206A>G (p.Glu402=)
NM_000178.4(GSS):c.1234C>A (p.Arg412=)
NM_000178.4(GSS):c.1252C>A (p.Arg418=)
NM_000178.4(GSS):c.1260C>G (p.Val420=) rs369657861
NM_000178.4(GSS):c.1260C>T (p.Val420=)
NM_000178.4(GSS):c.1272A>G (p.Ser424=)
NM_000178.4(GSS):c.1276C>T (p.Leu426=)
NM_000178.4(GSS):c.1281C>T (p.Gly427=)
NM_000178.4(GSS):c.129+10T>G
NM_000178.4(GSS):c.129+16C>T
NM_000178.4(GSS):c.129+17T>C
NM_000178.4(GSS):c.129+18C>A
NM_000178.4(GSS):c.129+19C>T
NM_000178.4(GSS):c.129+9C>G
NM_000178.4(GSS):c.130-12T>C
NM_000178.4(GSS):c.130-15_130-14insTA
NM_000178.4(GSS):c.130-18C>T
NM_000178.4(GSS):c.130-8G>A
NM_000178.4(GSS):c.1301+13G>A rs111816203
NM_000178.4(GSS):c.1301+15A>G
NM_000178.4(GSS):c.1302-11C>T
NM_000178.4(GSS):c.1302-14C>G
NM_000178.4(GSS):c.1302-15C>T
NM_000178.4(GSS):c.1302-16G>A
NM_000178.4(GSS):c.1302-16G>C
NM_000178.4(GSS):c.1302-18C>T
NM_000178.4(GSS):c.1305G>A (p.Gln435=)
NM_000178.4(GSS):c.1317C>T (p.Leu439=)
NM_000178.4(GSS):c.1329G>A (p.Lys443=)
NM_000178.4(GSS):c.132G>A (p.Val44=)
NM_000178.4(GSS):c.1332C>T (p.His444=)
NM_000178.4(GSS):c.1344A>T (p.Leu448=)
NM_000178.4(GSS):c.1353C>G (p.Thr451=)
NM_000178.4(GSS):c.135G>A (p.Val45=)
NM_000178.4(GSS):c.1374T>C (p.Asp458=)
NM_000178.4(GSS):c.1389G>A (p.Ala463=)
NM_000178.4(GSS):c.1422G>T (p.Val474=) rs367953336
NM_000178.4(GSS):c.153G>A (p.Thr51=)
NM_000178.4(GSS):c.156C>T (p.Leu52=)
NM_000178.4(GSS):c.183G>A (p.Leu61=)
NM_000178.4(GSS):c.189G>A (p.Glu63=)
NM_000178.4(GSS):c.198T>C (p.Tyr66=)
NM_000178.4(GSS):c.201T>C (p.Ala67=)
NM_000178.4(GSS):c.207G>A (p.Gln69=)
NM_000178.4(GSS):c.216C>T (p.Phe72=)
NM_000178.4(GSS):c.223C>T (p.Leu75=)
NM_000178.4(GSS):c.225A>G (p.Leu75=)
NM_000178.4(GSS):c.243G>A (p.Gln81=)
NM_000178.4(GSS):c.252C>A (p.Ala84=) rs1413763789
NM_000178.4(GSS):c.255C>T (p.Phe85=)
NM_000178.4(GSS):c.256C>T (p.Leu86=)
NM_000178.4(GSS):c.273C>G (p.Ser91=)
NM_000178.4(GSS):c.275+12T>C
NM_000178.4(GSS):c.275+19T>C
NM_000178.4(GSS):c.275+20T>C
NM_000178.4(GSS):c.275+20del rs770029537
NM_000178.4(GSS):c.275+7del rs768555177
NM_000178.4(GSS):c.276-16C>T
NM_000178.4(GSS):c.276-7C>T
NM_000178.4(GSS):c.282C>T (p.Ile94=)
NM_000178.4(GSS):c.306T>A (p.Arg102=)
NM_000178.4(GSS):c.315C>T (p.Asp105=)
NM_000178.4(GSS):c.318C>T (p.Ile106=)
NM_000178.4(GSS):c.330C>A (p.Val110=)
NM_000178.4(GSS):c.333A>G (p.Leu111=) rs2147130019
NM_000178.4(GSS):c.351+12C>T
NM_000178.4(GSS):c.351+20C>T
NM_000178.4(GSS):c.351+7A>G
NM_000178.4(GSS):c.354T>C (p.Thr118=)
NM_000178.4(GSS):c.357G>A (p.Val119=)
NM_000178.4(GSS):c.360C>T (p.Phe120=)
NM_000178.4(GSS):c.361C>T (p.Leu121=)
NM_000178.4(GSS):c.363G>C (p.Leu121=)
NM_000178.4(GSS):c.366C>T (p.Gly122=)
NM_000178.4(GSS):c.396C>T (p.Arg132=)
NM_000178.4(GSS):c.411C>T (p.Ser137=)
NM_000178.4(GSS):c.429C>A (p.Ile143=)
NM_000178.4(GSS):c.429C>T (p.Ile143=) rs145606015
NM_000178.4(GSS):c.42G>A (p.Gln14=)
NM_000178.4(GSS):c.438C>T (p.Asn146=)
NM_000178.4(GSS):c.462C>T (p.Gly154=) rs1326342374
NM_000178.4(GSS):c.477C>A (p.Thr159=)
NM_000178.4(GSS):c.477C>T (p.Thr159=) rs143272537
NM_000178.4(GSS):c.480A>T (p.Pro160=)
NM_000178.4(GSS):c.491+14G>A
NM_000178.4(GSS):c.492-5A>G
NM_000178.4(GSS):c.492-7C>T
NM_000178.4(GSS):c.531C>G (p.Gly177=)
NM_000178.4(GSS):c.537C>T (p.Ile179=)
NM_000178.4(GSS):c.540C>T (p.Leu180=)
NM_000178.4(GSS):c.608+13A>T
NM_000178.4(GSS):c.609-16T>G
NM_000178.4(GSS):c.609-18C>T
NM_000178.4(GSS):c.609-4C>G
NM_000178.4(GSS):c.609-6C>G
NM_000178.4(GSS):c.612T>C (p.Ala204=)
NM_000178.4(GSS):c.615G>C (p.Leu205=)
NM_000178.4(GSS):c.636G>A (p.Glu212=)
NM_000178.4(GSS):c.663T>G (p.Arg221=)
NM_000178.4(GSS):c.66C>G (p.Ala22=)
NM_000178.4(GSS):c.66C>T (p.Ala22=)
NM_000178.4(GSS):c.681A>G (p.Leu227=)
NM_000178.4(GSS):c.689+11del
NM_000178.4(GSS):c.689+14G>C
NM_000178.4(GSS):c.689+17G>A
NM_000178.4(GSS):c.689+17G>C
NM_000178.4(GSS):c.689+8A>G
NM_000178.4(GSS):c.689+9A>G
NM_000178.4(GSS):c.689+9A>T
NM_000178.4(GSS):c.690-12C>T
NM_000178.4(GSS):c.690-14C>T
NM_000178.4(GSS):c.690-17T>C
NM_000178.4(GSS):c.690-6T>C
NM_000178.4(GSS):c.690-8T>G
NM_000178.4(GSS):c.702G>C (p.Val234=) rs2147125544
NM_000178.4(GSS):c.723T>C (p.Asp241=)
NM_000178.4(GSS):c.738G>T (p.Gly246=)
NM_000178.4(GSS):c.759G>A (p.Arg253=)
NM_000178.4(GSS):c.767+12C>T
NM_000178.4(GSS):c.767+8T>G
NM_000178.4(GSS):c.768-11C>T
NM_000178.4(GSS):c.768-11del
NM_000178.4(GSS):c.768-12C>T
NM_000178.4(GSS):c.768-16C>G
NM_000178.4(GSS):c.786T>C (p.Ala262=)
NM_000178.4(GSS):c.789G>A (p.Val263=)
NM_000178.4(GSS):c.807C>T (p.Gly269=)
NM_000178.4(GSS):c.834+13T>C
NM_000178.4(GSS):c.834+8T>A
NM_000178.4(GSS):c.835-19T>C
NM_000178.4(GSS):c.835-8C>T
NM_000178.4(GSS):c.879G>A (p.Lys293=) rs2147122502
NM_000178.4(GSS):c.87G>A (p.Glu29=)
NM_000178.4(GSS):c.90A>T (p.Gly30=) rs1182355087
NM_000178.4(GSS):c.915G>A (p.Lys305=)
NM_000178.4(GSS):c.930G>A (p.Glu310=)
NM_000178.4(GSS):c.942G>A (p.Pro314=)
NM_000178.4(GSS):c.969C>G (p.Gly323=)
NM_000178.4(GSS):c.969C>T (p.Gly323=)
NM_000178.4(GSS):c.990C>T (p.Arg330=)
NM_000178.4(GSS):c.996C>T (p.Arg332=)

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