ClinVar Miner

List of variants in gene SARS2 studied for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 32
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HGVS dbSNP
NM_001145901.2(SARS2):c.*140C>T rs565577459
NM_001145901.2(SARS2):c.*22C>A rs199819134
NM_001145901.2(SARS2):c.*22C>T rs199819134
NM_001145901.2(SARS2):c.*79G>C rs9403
NM_001145901.2(SARS2):c.103A>G (p.Thr35Ala) rs34264048
NM_001145901.2(SARS2):c.1048T>C (p.Phe350Leu) rs1114167285
NM_001145901.2(SARS2):c.1166+4T>C rs7508411
NM_001145901.2(SARS2):c.1175A>G (p.Asp392Gly) rs727502784
NM_001145901.2(SARS2):c.1327G>A (p.Ala443Thr) rs762422369
NM_001145901.2(SARS2):c.1353+10G>A rs376335678
NM_001145901.2(SARS2):c.175G>C (p.Asp59His) rs886054430
NM_001145901.2(SARS2):c.248C>T (p.Ser83Leu) rs34050897
NM_001145901.2(SARS2):c.30G>A (p.Trp10Ter) rs145754412
NM_001145901.2(SARS2):c.310C>T (p.Arg104Trp) rs144760517
NM_001145901.2(SARS2):c.321G>A (p.Glu107=) rs11544093
NM_001145901.2(SARS2):c.353G>A (p.Arg118Gln) rs377601567
NM_001145901.2(SARS2):c.364-7C>A rs528674259
NM_001145901.2(SARS2):c.44G>C (p.Arg15Pro) rs773524954
NM_001145901.2(SARS2):c.471-76C>G rs886054429
NM_001145901.2(SARS2):c.507G>A (p.Ala169=) rs140304897
NM_001145901.2(SARS2):c.540+10G>A rs531462148
NM_001145901.2(SARS2):c.541-15G>C rs886054428
NM_001145901.2(SARS2):c.595+4G>A rs772644235
NM_001145901.2(SARS2):c.596-5T>A rs370612303
NM_001145901.2(SARS2):c.660-11C>G rs200300920
NM_001145901.2(SARS2):c.700C>T (p.Arg234Cys) rs201347156
NM_001145901.2(SARS2):c.764G>A (p.Arg255Gln) rs185053576
NM_001145901.2(SARS2):c.894G>A (p.Leu298=) rs182484523
NM_001145901.2(SARS2):c.923-4C>T rs542117712
NM_001145901.2(SARS2):c.969-10T>C rs749126576
NM_017827.3(SARS2):c.*341G>C rs374281807
NM_017827.3(SARS2):c.916+14_916+15delTG rs60352446

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