ClinVar Miner

List of variants reported as benign for obsolete accelerated tumor formation, susceptibility to by Invitae

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 14
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HGVS dbSNP gnomAD frequency
NC_000012.12:g.68808017C>G rs937282 0.56668
NM_002392.6(MDM2):c.-94A>G rs937283 0.36928
NM_002392.6(MDM2):c.14+309T>G rs2279744 0.30651
NM_002392.6(MDM2):c.14+55C>T rs2870820 0.29629
NM_002392.6(MDM2):c.1080A>G (p.Glu360=) rs769412 0.07570
NM_002392.6(MDM2):c.14+285G>C rs117039649 0.02270
NM_002392.6(MDM2):c.607C>T (p.Leu203=) rs1795480 0.01920
NM_002392.6(MDM2):c.100-10C>A rs56410897 0.00640
NM_002392.6(MDM2):c.918+15A>T rs565963964 0.00005
NM_002392.6(MDM2):c.15-9del rs555886264
NM_002392.6(MDM2):c.15-9dup rs555886264
NM_002392.6(MDM2):c.685-3del
NM_002392.6(MDM2):c.840+14del rs533467429
NM_002392.6(MDM2):c.99+12del

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