ClinVar Miner

List of variants in gene SLC37A4 reported as benign for carbohydrate metabolism disease

Included ClinVar conditions (161):
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Gene type:
ClinVar version:
Total variants: 24
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HGVS dbSNP
NM_001164277.1(SLC37A4):c.*125G>C rs8301
NM_001164277.1(SLC37A4):c.*418T>C rs11006
NM_001164277.1(SLC37A4):c.-420G>C rs2846281
NM_001164277.1(SLC37A4):c.-516G>A rs3759012
NM_001164277.1(SLC37A4):c.-755T>A rs1784559
NM_001164277.1(SLC37A4):c.1062C>T (p.Asn354=) rs61730035
NM_001164277.1(SLC37A4):c.1067G>C (p.Ser356Thr) rs547488738
NM_001164277.1(SLC37A4):c.1224G>A (p.Thr408=) rs8192696
NM_001164277.1(SLC37A4):c.1225G>A (p.Ala409Thr) rs886047748
NM_001164277.1(SLC37A4):c.1275C>T (p.Ser425=) rs35010541
NM_001164277.1(SLC37A4):c.1278G>A (p.Lys426=) rs34871377
NM_001164277.1(SLC37A4):c.149-14A>G rs79849261
NM_001164277.1(SLC37A4):c.183T>C (p.Ala61=) rs34123220
NM_001164277.1(SLC37A4):c.467C>T (p.Ala156Val) rs201036248
NM_001164277.1(SLC37A4):c.497G>A (p.Arg166His) rs186476316
NM_001164277.1(SLC37A4):c.593A>T (p.Asn198Ile) rs34203644
NM_001164277.1(SLC37A4):c.625+14C>T rs56394886
NM_001164277.1(SLC37A4):c.625+19C>T rs741811
NM_001164277.1(SLC37A4):c.781G>A (p.Val261Ile) rs561701030
NM_001164277.1(SLC37A4):c.968C>T (p.Thr323Ile) rs202209699
NM_001164277.1(SLC37A4):c.991A>G (p.Ile331Val) rs201967384
NM_001164277.2(SLC37A4):c.626+16G>A
NM_001467.6(SLC37A4):c.-195-64C>T rs56258965
NM_001467.6(SLC37A4):c.527= (p.Cys176=) rs56966114

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