ClinVar Miner

List of variants in gene SMC1A reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 25
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HGVS dbSNP
NM_006306.3(SMC1A):c.*1028C>T rs1057515967
NM_006306.3(SMC1A):c.*1240A>G rs1057515966
NM_006306.3(SMC1A):c.*1559G>A rs782736361
NM_006306.3(SMC1A):c.*1961C>T rs986586627
NM_006306.3(SMC1A):c.*2050T>C rs1057515964
NM_006306.3(SMC1A):c.*2225G>A rs1047323522
NM_006306.3(SMC1A):c.*2435T>G rs782650092
NM_006306.3(SMC1A):c.*2490T>C rs1057515962
NM_006306.3(SMC1A):c.*2663C>T rs1057515961
NM_006306.3(SMC1A):c.*3305A>G rs1057515960
NM_006306.3(SMC1A):c.*348C>T rs782700234
NM_006306.3(SMC1A):c.*3671C>T rs1057515959
NM_006306.3(SMC1A):c.*3777C>G rs41315082
NM_006306.3(SMC1A):c.*3807G>A rs1057515958
NM_006306.3(SMC1A):c.*4087G>A rs1057515957
NM_006306.3(SMC1A):c.*4382A>G rs906340789
NM_006306.3(SMC1A):c.*4443G>A rs782630117
NM_006306.3(SMC1A):c.*4581T>C rs1057515955
NM_006306.3(SMC1A):c.*5352C>T rs1057515953
NM_006306.3(SMC1A):c.*5355G>A rs782143840
NM_006306.3(SMC1A):c.*5692G>A rs1057515952
NM_006306.3(SMC1A):c.*5915T>C rs1057515951
NM_006306.3(SMC1A):c.*626A>G rs1057515970
NM_006306.3(SMC1A):c.*665A>G rs1057515969
NM_006306.3(SMC1A):c.*821_*824delACAG rs1057515968

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