ClinVar Miner

List of variants in gene GNS reported as benign for bone disorder

Included ClinVar conditions (1346):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 31
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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.793-68G>C rs1690277 0.68800
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.*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.21C>G (p.Ala7=) rs61743823 0.00937
NM_002076.4(GNS):c.1598G>A (p.Arg533His) rs61743822 0.00929
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.792+16A>G rs148924072 0.00415
NM_002076.4(GNS):c.1026G>A (p.Gln342=) rs115586725 0.00349
NM_002076.4(GNS):c.1113C>T (p.Asn371=) rs116798538 0.00279
NM_002076.4(GNS):c.193-9C>T rs372633889 0.00008
NM_002076.4(GNS):c.876-13T>C rs543570530 0.00006
NM_002076.4(GNS):c.1155C>A (p.Asp385Glu) rs755021062 0.00003
NM_002076.4(GNS):c.285A>G (p.Arg95=) rs545765198 0.00002
NM_002076.4(GNS):c.253-10del rs201654719
NM_002076.4(GNS):c.526-6del rs2136248435
NM_002076.4(GNS):c.625-10dup rs2136247672
NM_002076.4(GNS):c.793-15del rs754323701
NM_002076.4(GNS):c.793-15dup

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