ClinVar Miner

List of variants in gene combination SNHG14, SNRPN reported as uncertain significance for autism spectrum disorder

Included ClinVar conditions (38):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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NM_022806.4(SNRPN):c.-579+6065del rs886051014
NM_022807.4(SNRPN):c.-504-12T>C rs886051015
NM_022807.4(SNRPN):c.-584A>G rs58890023
NM_022807.4(SNRPN):c.-636C>A rs886051013
NM_022807.4(SNRPN):c.-819C>A rs886051012
NM_022807.4(SNRPN):c.-823T>C rs886051011
NM_022807.4(SNRPN):c.-841T>A rs886051010

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