ClinVar Miner

List of variants in gene GNS reported as benign for carbohydrate metabolism disease

Included ClinVar conditions (161):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 25
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HGVS dbSNP
NM_002076.4(GNS):c.*1228C>T rs115625510
NM_002076.4(GNS):c.*1353G>A rs1269548
NM_002076.4(GNS):c.*1456C>T rs144199387
NM_002076.4(GNS):c.*1648C>T rs75568735
NM_002076.4(GNS):c.*1990A>G rs17100600
NM_002076.4(GNS):c.*2361C>G rs1061743
NM_002076.4(GNS):c.*269C>T rs2279597
NM_002076.4(GNS):c.*380C>T rs674
NM_002076.4(GNS):c.*411G>A rs11175525
NM_002076.4(GNS):c.*566A>G rs17100604
NM_002076.4(GNS):c.*814T>C
NM_002076.4(GNS):c.*942A>G rs12309081
NM_002076.4(GNS):c.1026G>A (p.Gln342=) rs115586725
NM_002076.4(GNS):c.1113C>T (p.Asn371=) rs116798538
NM_002076.4(GNS):c.1598G>A (p.Arg533His) rs61743822
NM_002076.4(GNS):c.1650T>C (p.His550=) rs2230292
NM_002076.4(GNS):c.193-9C>T rs372633889
NM_002076.4(GNS):c.198G>A (p.Pro66=) rs1147096
NM_002076.4(GNS):c.21C>G (p.Ala7=) rs61743823
NM_002076.4(GNS):c.253-10del rs201654719
NM_002076.4(GNS):c.285A>G (p.Arg95=) rs545765198
NM_002076.4(GNS):c.363G>A (p.Lys121=) rs2230291
NM_002076.4(GNS):c.459+14T>C rs78614637
NM_002076.4(GNS):c.526-6del
NM_002076.4(GNS):c.792+16A>G

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