ClinVar Miner

List of variants in gene SPRED1 reported as benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
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NM_152594.3(SPRED1):c.*1724A>C rs1554527
NM_152594.3(SPRED1):c.*248T>C rs16966842
NM_152594.3(SPRED1):c.*256C>T rs145373657
NM_152594.3(SPRED1):c.*2831G>A rs35490364
NM_152594.3(SPRED1):c.*3521A>G rs11634702
NM_152594.3(SPRED1):c.*3698T>G rs76527876
NM_152594.3(SPRED1):c.*3830G>A rs8039150
NM_152594.3(SPRED1):c.*3946G>A rs8039337
NM_152594.3(SPRED1):c.*3996G>A rs72725364
NM_152594.3(SPRED1):c.*427A>T rs185290497
NM_152594.3(SPRED1):c.*4662T>A rs10852019
NM_152594.3(SPRED1):c.*4932A>G rs16966843
NM_152594.3(SPRED1):c.*5110C>T rs8026118
NM_152594.3(SPRED1):c.-244T>C rs138385793
NM_152594.3(SPRED1):c.-93C>T rs192699510
NM_152594.3(SPRED1):c.1044T>C (p.Val348=) rs3751526
NM_152594.3(SPRED1):c.291G>A (p.Lys97=) rs7182445
NM_152594.3(SPRED1):c.424-8C>A rs7180446
NM_152594.3(SPRED1):c.583-7A>G rs115970207
NM_152594.3(SPRED1):c.926T>C (p.Val309Ala) rs114636635

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