ClinVar Miner

List of variants in gene SLC37A4 reported as benign for not provided

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Gene type:
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Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_001164277.1(SLC37A4):c.-755T>A rs1784559 0.50768
NM_001164277.2(SLC37A4):c.*125G>C rs8301 0.28518
NM_001164277.2(SLC37A4):c.-195-136A>C rs58412813 0.28510
NM_001164277.2(SLC37A4):c.986-76T>C rs2276072 0.20754
NM_001164277.2(SLC37A4):c.986-77T>G rs2276071 0.20745
NM_001164277.2(SLC37A4):c.-195-64C>T rs56258965 0.15980
NM_001164277.2(SLC37A4):c.148+215C>T rs61902084 0.06227
NM_001164277.2(SLC37A4):c.-195-89C>T rs11217128 0.05282
NM_001164277.2(SLC37A4):c.-700+31A>C rs75634142 0.04103
NM_001164277.2(SLC37A4):c.626+76C>T rs79511838 0.04103
NM_001164277.2(SLC37A4):c.871+50C>T rs78121950 0.03427
NM_001164277.2(SLC37A4):c.786-74T>C rs73559193 0.03303
NM_001164277.2(SLC37A4):c.148+174G>A rs80235222 0.03062
NM_001164277.2(SLC37A4):c.871+51G>A rs77180649 0.02934
NC_000011.10:g.119030939C>A rs114116089 0.02158
NM_001164277.2(SLC37A4):c.626+102G>A rs73559195 0.01903
NM_001164277.2(SLC37A4):c.149-14A>G rs79849261 0.01232
NM_001164277.2(SLC37A4):c.1275C>T (p.Ser425=) rs35010541 0.01045
NM_001164277.2(SLC37A4):c.1062C>T (p.Asn354=) rs61730035 0.00758
NM_001164277.2(SLC37A4):c.593A>T (p.Asn198Ile) rs34203644 0.00280
NM_001164277.2(SLC37A4):c.968C>T (p.Thr323Ile) rs202209699 0.00273
NM_001164277.2(SLC37A4):c.467C>T (p.Ala156Val) rs201036248 0.00214
NM_001164277.2(SLC37A4):c.*17G>A rs782225728 0.00002
NM_001164277.2(SLC37A4):c.149-82G>A rs4936459
NM_001164277.2(SLC37A4):c.527= (p.Cys176=) rs56966114
NM_001164277.2(SLC37A4):c.627-157G>A rs74888816
NM_001164277.2(SLC37A4):c.872-169C>T rs57156480
NM_001164277.2(SLC37A4):c.985+247C>T

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