ClinVar Miner

List of variants reported as benign for gastric cancer by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (25):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_000038.6(APC):c.4479G>A (p.Thr1493=) rs41115 0.59177
NM_004360.5(CDH1):c.1849G>A (p.Ala617Thr) rs33935154 0.01412
NM_004360.5(CDH1):c.-71C>G rs34033771 0.00927
NM_000038.6(APC):c.4326T>A (p.Pro1442=) rs67622085 0.00705
NM_001048174.2(MUTYH):c.1347G>C (p.Thr449=) rs74318065 0.00596
NM_000141.5(FGFR2):c.17G>C (p.Arg6Pro) rs3750819 0.00250

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