ClinVar Miner

List of variants in gene ZFP57 reported as uncertain significance for digestive system disorder

Included ClinVar conditions (605):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_001109809.5(ZFP57):c.1033G>C (p.Ala345Pro) rs200537697 0.00211
NM_001109809.5(ZFP57):c.475A>T (p.Thr159Ser) rs201703858 0.00211
NM_001109809.5(ZFP57):c.532T>C (p.Tyr178His) rs146835830 0.00210
NM_001109809.5(ZFP57):c.1472C>G (p.Thr491Ser) rs184974475 0.00159
NM_001109809.5(ZFP57):c.285C>T (p.Thr95=) rs373253380 0.00014
NM_001109809.5(ZFP57):c.749G>A (p.Arg250His) rs199589695 0.00007
NM_001109809.5(ZFP57):c.553A>G (p.Ser185Gly) rs755902229 0.00006
NM_001109809.5(ZFP57):c.277C>G (p.Leu93Val) rs369213004 0.00005
NM_001109809.5(ZFP57):c.752G>A (p.Arg251His) rs774050037 0.00004
NM_001109809.5(ZFP57):c.495G>A (p.Val165=) rs771387494 0.00003
NM_001109809.5(ZFP57):c.1230G>A (p.Pro410=) rs578187010 0.00001
NM_001109809.5(ZFP57):c.798G>A (p.Lys266=) rs886061285 0.00001
NM_001109809.5(ZFP57):c.826C>T (p.Arg276Cys) rs552912198 0.00001
NM_001109809.5(ZFP57):c.288G>C (p.Lys96Asn) rs745602868
NM_001109809.5(ZFP57):c.374G>A (p.Arg125Gln) rs114591600
NM_001109809.5(ZFP57):c.724G>T (p.Asp242Tyr) rs1554211826
NM_001109809.5(ZFP57):c.751C>T (p.Arg251Cys)
NM_001109809.5(ZFP57):c.857C>T (p.Pro286Leu) rs753928819

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