ClinVar Miner

List of variants in gene combination LOC126859837, SYNE1 reported as benign for autosomal recessive disease

Included ClinVar conditions (1198):
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_182961.4(SYNE1):c.17202+24G>A rs12662994 0.09437
NM_182961.4(SYNE1):c.16896+20del rs545568394
NM_182961.4(SYNE1):c.16896+9dup rs761957607

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