ClinVar Miner

List of variants in gene LYST reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP
NC_000001.11:g.235693239dup rs5781839
NM_000081.4(LYST):c.1251A>G (p.Gln417=) rs1063128
NM_000081.4(LYST):c.1683A>G (p.Leu561=) rs3820553
NM_000081.4(LYST):c.4956A>G (p.Leu1652=) rs6696123
NM_000081.4(LYST):c.5373G>A (p.Lys1791=) rs2273584
NM_000081.4(LYST):c.6122-13del rs201404906
NM_001301365.1(LYST):c.10564+43G>A rs7541057
NM_001301365.1(LYST):c.10701+255T>G rs12122253
NM_001301365.1(LYST):c.10701+316C>T rs116553564
NM_001301365.1(LYST):c.11195+124G>A rs12092604
NM_001301365.1(LYST):c.153A>C (p.Gly51=) rs11464
NM_001301365.1(LYST):c.193-233G>A rs7529320
NM_001301365.1(LYST):c.193-290A>G rs7522053
NM_001301365.1(LYST):c.2316C>T (p.Asp772=) rs16832868
NM_001301365.1(LYST):c.4863-115T>C rs2011390
NM_001301365.1(LYST):c.5785-307G>A rs6668388
NM_001301365.1(LYST):c.5847G>C (p.Gln1949His) rs6665568
NM_001301365.1(LYST):c.6630A>G (p.Glu2210=) rs34466404
NM_001301365.1(LYST):c.7793T>A (p.Phe2598Tyr) rs34642241
NM_001301365.1(LYST):c.8151+296A>G rs2753329
NM_001301365.1(LYST):c.8801+77G>A rs6429275
NM_001301365.1(LYST):c.9315+52C>A rs6667717
NM_001301365.1(LYST):c.9926-57A>G rs2275856

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