ClinVar Miner

List of variants in gene SKIV2L reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (891):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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HGVS dbSNP
NM_006929.4(SKIV2L):c.*19T>C rs2075702
NM_006929.4(SKIV2L):c.1041C>T (p.Ala347=) rs35664695
NM_006929.4(SKIV2L):c.1200A>G (p.Thr400=) rs2734331
NM_006929.4(SKIV2L):c.2211G>A (p.Pro737=) rs2280773
NM_006929.4(SKIV2L):c.2659G>A (p.Asp887Asn) rs3911893
NM_006929.4(SKIV2L):c.2749G>A (p.Val917Met) rs106287
NM_006929.4(SKIV2L):c.452A>G (p.Gln151Arg) rs438999

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