ClinVar Miner

List of variants in gene SLC37A4 reported as likely benign for not specified

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Gene type:
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Total variants: 13
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HGVS dbSNP
NM_001164277.1(SLC37A4):c.*11G>A rs978301169
NM_001164277.1(SLC37A4):c.-183C>T rs145369754
NM_001164277.1(SLC37A4):c.-196+14C>T rs1555192097
NM_001164277.1(SLC37A4):c.-700+10G>T rs1057522895
NM_001164277.1(SLC37A4):c.-700+9C>T rs534659292
NM_001164277.1(SLC37A4):c.1067G>C (p.Ser356Thr) rs547488738
NM_001164277.1(SLC37A4):c.1098C>T (p.His366=) rs782587864
NM_001164277.1(SLC37A4):c.150G>T (p.Gly50=) rs202137454
NM_001164277.1(SLC37A4):c.381+15A>G rs1057520372
NM_001164277.1(SLC37A4):c.540C>T (p.Ser180=) rs371716153
NM_001164277.1(SLC37A4):c.593A>T (p.Asn198Ile) rs34203644
NM_001164277.1(SLC37A4):c.784+6A>T rs369358436
NM_001164277.1(SLC37A4):c.785-7A>G rs781887799

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