List of variants in gene SRP72 reported as uncertain significance for immune system disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 38

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HGVS	dbSNP	gnomAD frequency
NM_006947.4(SRP72):c.*606A>T	rs868279024	0.05397
NM_006947.4(SRP72):c.*221A>G	rs149250989	0.00152
NM_006947.4(SRP72):c.*194G>A	rs188713088	0.00073
NM_006947.4(SRP72):c.*505C>T	rs562987091	0.00031
NM_006947.4(SRP72):c.*624A>G	rs867685822	0.00025
NM_006947.4(SRP72):c.*1385A>G	rs754461786	0.00022
NM_006947.4(SRP72):c.*635C>T	rs200981113	0.00015
NM_006947.4(SRP72):c.622C>T (p.Arg208Cys)	rs375436807	0.00011
NM_006947.4(SRP72):c.623G>A (p.Arg208His)	rs369761160	0.00011
NM_006947.4(SRP72):c.*839T>C	rs757066668	0.00009
NM_006947.4(SRP72):c.*1483A>G	rs566533583	0.00008
NM_006947.4(SRP72):c.*321A>G	rs886059499	0.00007
NM_006947.4(SRP72):c.*622G>A	rs775675334	0.00007
NM_006947.4(SRP72):c.*1241C>T	rs1282273094	0.00006
NM_006947.4(SRP72):c.*1678C>T	rs886059503	0.00003
NM_006947.4(SRP72):c.*1764A>G	rs192226722	0.00003
NM_006947.4(SRP72):c.*1478C>A	rs1405583789	0.00002
NM_006947.4(SRP72):c.1636C>A (p.Gln546Lys)	rs1185247120	0.00002
NM_006947.4(SRP72):c.*227G>A	rs879875987	0.00001
NM_006947.4(SRP72):c.*473G>A	rs1020026480	0.00001
NM_006947.4(SRP72):c.973A>G (p.Lys325Glu)	rs763655714	0.00001
NM_006947.4(SRP72):c.1227_1232del	rs886059502
NM_006947.4(SRP72):c.*125GT[1]	rs886059498
NM_006947.4(SRP72):c.*142A>G	rs878964615
NM_006947.4(SRP72):c.*1769T>G	rs886059504
NM_006947.4(SRP72):c.*407T>C	rs541665813
NM_006947.4(SRP72):c.*606AT[10]	rs201131530
NM_006947.4(SRP72):c.*633T>C	rs867120149
NM_006947.4(SRP72):c.*637TA[11]	rs35852754
NM_006947.4(SRP72):c.*637TA[7]	rs35852754
NM_006947.4(SRP72):c.*637TA[9]	rs35852754
NM_006947.4(SRP72):c.1843G>T (p.Ala615Ser)
NM_006947.4(SRP72):c.1900G>C (p.Val634Leu)
NM_006947.4(SRP72):c.1938C>G (p.His646Gln)	rs1721270142
NM_006947.4(SRP72):c.308G>A (p.Ser103Asn)
NM_006947.4(SRP72):c.50A>G (p.Glu17Gly)
NM_006947.4(SRP72):c.574C>G (p.Leu192Val)	rs772592244
NM_006947.4(SRP72):c.979T>C (p.Ser327Pro)	rs1040868057

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