ClinVar Miner

List of variants in gene GNS reported by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 87
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HGVS dbSNP gnomAD frequency
NM_002076.4(GNS):c.198G>A (p.Pro66=) rs1147096 0.70681
NM_002076.4(GNS):c.*380C>T rs674 0.63058
NM_002076.4(GNS):c.*2361C>G rs1061743 0.52503
NM_002076.4(GNS):c.*1353G>A rs1269548 0.51078
NM_002076.4(GNS):c.*269C>T rs2279597 0.21062
NM_002076.4(GNS):c.363G>A (p.Lys121=) rs2230291 0.09139
NM_002076.4(GNS):c.*942A>G rs12309081 0.06453
NM_002076.4(GNS):c.*411G>A rs11175525 0.06452
NM_002076.4(GNS):c.*3068_*3069dup rs397946778 0.04705
NM_002076.4(GNS):c.*1990A>G rs17100600 0.04306
NM_002076.4(GNS):c.*566A>G rs17100604 0.04303
NM_002076.4(GNS):c.1650T>C (p.His550=) rs2230292 0.03695
NM_002076.4(GNS):c.*1456C>T rs144199387 0.01725
NM_002076.4(GNS):c.459+14T>C rs78614637 0.01673
NM_002076.4(GNS):c.*599T>A rs151304792 0.01029
NM_002076.4(GNS):c.21C>G (p.Ala7=) rs61743823 0.00937
NM_002076.4(GNS):c.1598G>A (p.Arg533His) rs61743822 0.00929
NM_002076.4(GNS):c.*2751C>T rs137943279 0.00886
NM_002076.4(GNS):c.*814T>C rs78614043 0.00798
NM_002076.4(GNS):c.*1228C>T rs115625510 0.00797
NM_002076.4(GNS):c.*1648C>T rs75568735 0.00795
NM_002076.4(GNS):c.1026G>A (p.Gln342=) rs115586725 0.00349
NM_002076.4(GNS):c.*2735C>T rs143396704 0.00233
NM_002076.4(GNS):c.*1681C>G rs142676698 0.00074
NM_002076.4(GNS):c.*1861del rs3832839 0.00061
NM_002076.4(GNS):c.*152G>A rs768957003 0.00041
NM_002076.4(GNS):c.*357T>C rs554471490 0.00041
NM_002076.4(GNS):c.4C>T (p.Arg2Trp) rs200441930 0.00033
NM_002076.4(GNS):c.*2301G>A rs141182054 0.00032
NM_002076.4(GNS):c.1434C>G (p.Val478=) rs141958901 0.00028
NM_002076.4(GNS):c.*676A>G rs886049769 0.00025
NM_002076.4(GNS):c.*1759A>G rs540594590 0.00024
NM_002076.4(GNS):c.*2099G>A rs553360517 0.00024
NM_002076.4(GNS):c.5G>C (p.Arg2Pro) rs759075764 0.00016
NM_002076.4(GNS):c.*2612G>T rs533328232 0.00012
NM_002076.4(GNS):c.*2843C>T rs577545481 0.00011
NM_002076.4(GNS):c.577C>T (p.Arg193Trp) rs144220755 0.00011
NM_002076.4(GNS):c.*2656G>A rs577212739 0.00009
NM_002076.4(GNS):c.624+10A>G rs757526895 0.00009
NM_002076.4(GNS):c.876-13T>C rs543570530 0.00006
NM_002076.4(GNS):c.*2278A>C rs1036841344 0.00005
NM_002076.4(GNS):c.*2844G>A rs534118009 0.00005
NM_002076.4(GNS):c.*2447G>A rs567930294 0.00004
NM_002076.4(GNS):c.*319C>T rs368523842 0.00004
NM_002076.4(GNS):c.*71T>C rs983471422 0.00004
NM_002076.4(GNS):c.*2032T>A rs886049763 0.00003
NM_002076.4(GNS):c.*2560T>G rs886049762 0.00003
NM_002076.4(GNS):c.*2625G>A rs1468841522 0.00003
NM_002076.4(GNS):c.*2783C>T rs573404754 0.00003
NM_002076.4(GNS):c.*425G>A rs141736156 0.00003
NM_002076.4(GNS):c.1153G>A (p.Asp385Asn) rs138335335 0.00003
NM_002076.4(GNS):c.*2740G>A rs886049761 0.00002
NM_002076.4(GNS):c.285A>G (p.Arg95=) rs545765198 0.00002
NM_002076.3(GNS):c.-161T>C rs769119181 0.00001
NM_002076.4(GNS):c.*1435G>A rs547333907 0.00001
NM_002076.4(GNS):c.*2571T>C rs995044057 0.00001
NM_002076.4(GNS):c.*2699G>C rs867153534 0.00001
NM_002076.4(GNS):c.*334C>T rs886049771 0.00001
NM_002076.4(GNS):c.*764G>A rs886049767 0.00001
NM_002076.4(GNS):c.*826G>A rs886049766 0.00001
NM_002076.4(GNS):c.*86A>T rs1868866389 0.00001
NM_002076.4(GNS):c.*985A>G rs531715804 0.00001
NM_002076.4(GNS):c.-83G>C rs1290374156 0.00001
NM_002076.4(GNS):c.1104G>T (p.Leu368=) rs766168524 0.00001
NM_002076.4(GNS):c.1261C>T (p.Arg421Cys) rs1177531995 0.00001
NM_002076.4(GNS):c.1616G>A (p.Arg539His) rs766615352 0.00001
NM_002076.4(GNS):c.337A>G (p.Thr113Ala) rs886049772 0.00001
NM_002076.4(GNS):c.73G>A (p.Ala25Thr) rs540537083 0.00001
NM_002076.3(GNS):c.-168dupC rs145477737
NM_002076.4(GNS):c.*1580A>G rs886049764
NM_002076.4(GNS):c.*1809T>C rs1868815358
NM_002076.4(GNS):c.*1977A>G rs1868809897
NM_002076.4(GNS):c.*2146G>A rs900823217
NM_002076.4(GNS):c.*2406A>G rs1868795917
NM_002076.4(GNS):c.*2489T>C rs529418480
NM_002076.4(GNS):c.*2611dup rs201933913
NM_002076.4(GNS):c.*2787del rs886049760
NM_002076.4(GNS):c.*37G>T rs142001509
NM_002076.4(GNS):c.*574G>A rs886049770
NM_002076.4(GNS):c.*699G>C rs1868848563
NM_002076.4(GNS):c.*734A>G rs886049768
NM_002076.4(GNS):c.*846C>T rs886049765
NM_002076.4(GNS):c.-120A>G rs778270030
NM_002076.4(GNS):c.-39TCCCG[4] rs559286032
NM_002076.4(GNS):c.16C>G (p.Leu6Val) rs746189087
NM_002076.4(GNS):c.229A>G (p.Met77Val) rs763723151
NM_002076.4(GNS):c.939T>G (p.Thr313=) rs1869657867

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