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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_003097.6(SNRPN):c.-89T>C	rs705	0.53733
NM_003097.6(SNRPN):c.-39G>A	rs75184959	0.01903
NM_003097.6(SNRPN):c.-378C>T	rs426541	0.01033
NM_003097.6(SNRPN):c.3+10A>G	rs112560608	0.00515
NM_003097.6(SNRPN):c.183T>C (p.Arg61=)	rs373215950	0.00031
NM_003097.6(SNRPN):c.-274G>A	rs142583293	0.00014
NM_003097.6(SNRPN):c.-86G>A	rs886051018	0.00011
NM_003097.6(SNRPN):c.-280C>T	rs372295822	0.00009
NM_003097.6(SNRPN):c.-20G>T	rs763736287	0.00005
NM_003097.6(SNRPN):c.-295+8C>G	rs371808119	0.00004
NM_003097.6(SNRPN):c.-110T>G	rs190439178	0.00001
NM_003097.6(SNRPN):c.-386C>T	rs776280755	0.00001
NM_003097.6(SNRPN):c.524C>T (p.Pro175Leu)	rs886051020	0.00001
NM_003097.6(SNRPN):c.-143-6C>T	rs886051017
NM_003097.6(SNRPN):c.-262A>T	rs765651266
NM_003097.6(SNRPN):c.-380C>T	rs886051016
NM_003097.6(SNRPN):c.421-5C>T	rs886051019

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