ClinVar Miner

List of variants in gene SNHG14, SNRPN, SNURF studied for autism spectrum disorder

Included ClinVar conditions (38):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
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NM_003097.5(SNRPN):c.183T>C (p.Arg61=) rs373215950
NM_003097.5(SNRPN):c.3+10A>G rs112560608
NM_022807.4(SNRPN):c.-110T>G rs190439178
NM_022807.4(SNRPN):c.-143-6C>T rs886051017
NM_022807.4(SNRPN):c.-20G>T rs763736287
NM_022807.4(SNRPN):c.-262A>T rs765651266
NM_022807.4(SNRPN):c.-274G>A rs142583293
NM_022807.4(SNRPN):c.-280C>T rs372295822
NM_022807.4(SNRPN):c.-295+8C>G rs371808119
NM_022807.4(SNRPN):c.-378C>T rs426541
NM_022807.4(SNRPN):c.-380C>T rs886051016
NM_022807.4(SNRPN):c.-386C>T rs776280755
NM_022807.4(SNRPN):c.-39G>A rs75184959
NM_022807.4(SNRPN):c.-86G>A rs886051018
NM_022807.4(SNRPN):c.-89T>C rs705
NM_022807.4(SNRPN):c.421-5C>T rs886051019
NM_022807.4(SNRPN):c.524C>T (p.Pro175Leu) rs886051020

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