List of variants in gene IL10, IL19 studied 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
		ClinVar version:

Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_000572.3(IL10):c.378+19T>C	rs1554286	0.73006
NM_000572.3(IL10):c.225+56A>G	rs1518111	0.70961
NC_000001.11:g.206773289A>G	rs1800871	0.69449
NC_000001.11:g.206773062T>G	rs1800872	0.69428
NM_000572.3(IL10):c.225+18G>A	rs376490444	0.00033
NM_000572.3(IL10):c.166-15T>C	rs191140520	0.00014
NM_000572.3(IL10):c.225+6A>G	rs749041176	0.00008
NM_000572.3(IL10):c.371G>A (p.Arg124Gln)	rs201365412	0.00004
NM_000572.3(IL10):c.374G>A (p.Arg125His)	rs374619208	0.00003
NM_000572.3(IL10):c.225+15G>A	rs1342823726	0.00002
NM_000572.3(IL10):c.225+17G>A	rs1674832645	0.00001
NM_000572.3(IL10):c.365G>A (p.Arg122Lys)	rs371608920	0.00001
NM_000572.3(IL10):c.370C>T (p.Arg124Trp)	rs746523858	0.00001
NC_000001.11:g.206775286T>C	rs587776843
NM_000572.3(IL10):c.166-19C>T
NM_000572.3(IL10):c.166-7C>T
NM_000572.3(IL10):c.201G>A (p.Lys67=)	rs2102439750
NM_000572.3(IL10):c.209T>A (p.Leu70Ter)	rs1558603013
NM_000572.3(IL10):c.213G>T (p.Leu71=)
NM_000572.3(IL10):c.225+20G>A
NM_000572.3(IL10):c.361C>T (p.Leu121=)
NM_000572.3(IL10):c.372G>A (p.Arg124=)
NM_000572.3(IL10):c.374G>T (p.Arg125Leu)	rs374619208
NM_000572.3(IL10):c.375C>A (p.Arg125=)	rs755403362
NM_000572.3(IL10):c.378+15A>C
NM_000572.3(IL10):c.378+16G>C
NM_000572.3(IL10):c.378+19_378+20delinsCC	rs2102439038
NM_000572.3(IL10):c.378+6T>C

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