List of variants in gene SLC2A1 reported as benign for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 30

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HGVS	dbSNP	gnomAD frequency
NM_006516.4(SLC2A1):c.-197A>C	rs11537640	0.23186
NM_006516.2(SLC2A1):c.-390delA	rs28365848	0.23160
NM_006516.4(SLC2A1):c.45C>T (p.Ala15=)	rs1385129	0.21537
NM_006516.4(SLC2A1):c.399C>T (p.Cys133=)	rs11537641	0.16943
NM_006516.4(SLC2A1):c.19-428G>A	rs35022307	0.15612
NM_006516.4(SLC2A1):c.19-187C>A	rs12718444	0.15574
NM_006516.4(SLC2A1):c.19-372A>G	rs34964576	0.15481
NM_006516.4(SLC2A1):c.1074+132T>C	rs72956801	0.06251
NM_006516.4(SLC2A1):c.1065A>G (p.Leu355=)	rs2228490	0.04552
NM_006516.4(SLC2A1):c.1074+118G>C	rs2306663	0.03773
NM_006516.4(SLC2A1):c.868-108T>G	rs74068369	0.03601
NM_006516.4(SLC2A1):c.1074+231C>G	rs74068367	0.03421
NM_006516.4(SLC2A1):c.1075-217G>A	rs74068366	0.02030
NM_006516.4(SLC2A1):c.-190G>C	rs114514007	0.01675
NM_006516.4(SLC2A1):c.19-207T>C	rs41310434	0.01173
NM_006516.4(SLC2A1):c.417C>T (p.Phe139=)	rs144538918	0.00517
NM_006516.4(SLC2A1):c.27G>A (p.Thr9=)	rs34025424	0.00176
NM_006516.4(SLC2A1):c.1372C>A (p.Arg458=)	rs13306758	0.00070
NM_006516.4(SLC2A1):c.777C>T (p.Ile259=)	rs78388808	0.00068
NM_006516.4(SLC2A1):c.276-50C>T	rs368610353	0.00054
NM_006516.4(SLC2A1):c.864C>T (p.Asn288=)	rs150384629	0.00047
NM_006516.4(SLC2A1):c.138G>C (p.Gln46His)	rs149998596	0.00014
NM_006516.4(SLC2A1):c.1005C>G (p.Thr335=)	rs763664146	0.00006
NM_006516.4(SLC2A1):c.1016T>C (p.Ile339Thr)	rs141619735	0.00006
NM_006516.4(SLC2A1):c.906G>T (p.Gly302=)	rs55693364	0.00004
NM_006516.4(SLC2A1):c.1155C>T (p.Pro385=)	rs76860965
NM_006516.4(SLC2A1):c.1278+30_1278+31insCTCACCATTT	rs3831326
NM_006516.4(SLC2A1):c.588G>A (p.Pro196=)	rs2229682
NM_006516.4(SLC2A1):c.679+7G>C	rs13306757
NM_006516.4(SLC2A1):c.972+25C>A	rs187701356

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