ClinVar Miner

List of variants in gene LOC130064579, MEGF8 studied for bone disorder

Included ClinVar conditions (1436):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_001271938.2(MEGF8):c.7C>T (p.Leu3=) rs371769004 0.00019
NM_001271938.2(MEGF8):c.27G>C (p.Met9Ile) rs1029623509 0.00001
NM_001271938.2(MEGF8):c.47C>G (p.Ala16Gly) rs1050352479

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