ClinVar Miner

List of variants in gene SLMAP reported as benign for cardiovascular disorder

Included ClinVar conditions (1426):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_001377540.1(SLMAP):c.967-979A>G rs9844865 0.33177
NM_001377540.1(SLMAP):c.1443C>T (p.Asp481=) rs17058639 0.23931
NM_001377540.1(SLMAP):c.828+11C>A rs2306056 0.19942
NM_001377540.1(SLMAP):c.1300+14A>G rs111294347 0.03108
NM_001377540.1(SLMAP):c.2145G>A (p.Gln715=) rs17745496 0.02362
NM_001377540.1(SLMAP):c.1968T>A (p.Leu656=) rs35219531 0.01667
NM_001377540.1(SLMAP):c.2064C>T (p.Thr688=) rs146313438 0.00301
NM_001377540.1(SLMAP):c.495A>G (p.Leu165=) rs149758819 0.00253
NM_001377540.1(SLMAP):c.829-15A>G rs142871558 0.00143
NM_001377540.1(SLMAP):c.1776T>C (p.Asp592=) rs554868355 0.00080
NM_001377540.1(SLMAP):c.2055A>G (p.Ala685=) rs141033845 0.00036
NM_001377540.1(SLMAP):c.1301-12T>C rs376904413 0.00023
NM_001377540.1(SLMAP):c.2020+20A>G rs202130040 0.00015
NM_001377540.1(SLMAP):c.1923T>C (p.Ser641=) rs373485907 0.00013
NM_001377540.1(SLMAP):c.297C>T (p.Ser99=) rs190769315 0.00006
NM_001377540.1(SLMAP):c.324C>T (p.Asp108=) rs541100817 0.00004
NM_001377540.1(SLMAP):c.1317A>G (p.Glu439=) rs189861519 0.00003
NM_001377540.1(SLMAP):c.1704A>G (p.Gln568=) rs771986392 0.00003
NM_001377540.1(SLMAP):c.828+10_828+11insA rs766631211 0.00003
NM_001377540.1(SLMAP):c.651A>G (p.Leu217=) rs74857771 0.00002
NM_001377540.1(SLMAP):c.828+11del rs113521063 0.00002
NM_001377540.1(SLMAP):c.1361-9del rs776085613
NM_001377540.1(SLMAP):c.199-5dup rs199960887
NM_001377540.1(SLMAP):c.2021-14del
NM_001377540.1(SLMAP):c.2311-14_2311-13del
NM_001377540.1(SLMAP):c.346+24dup rs771836522
NM_001377540.1(SLMAP):c.419+29_419+39del rs748357817
NM_001377540.1(SLMAP):c.420-17T>A
NM_001377540.1(SLMAP):c.828+21del rs760021345
NM_001377540.1(SLMAP):c.828+21dup rs760021345

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