ClinVar Miner

List of variants in gene MYL2 reported as benign by GeneDx

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_000432.4(MYL2):c.170-160C>G rs34254113 0.21528
NM_000432.4(MYL2):c.403-244T>C rs12231049 0.13992
NM_000432.4(MYL2):c.94-168G>A rs61942999 0.12075
NM_000432.4(MYL2):c.132T>C (p.Ile44=) rs2301610 0.08171
NM_000432.4(MYL2):c.402+245T>C rs3782889 0.06943
NM_000432.4(MYL2):c.402+129G>A rs3825389 0.06928
NM_000432.4(MYL2):c.274+53G>A rs11065770 0.05569
NM_000432.4(MYL2):c.353+47del rs369884745 0.03692
NM_000432.4(MYL2):c.381G>A (p.Ala127=) rs2233261 0.00558
NM_000432.4(MYL2):c.170-19T>C rs115522476 0.00399
NM_000432.4(MYL2):c.279G>A (p.Ala93=) rs28645088 0.00131
NM_000432.4(MYL2):c.*127C>T rs546464364 0.00037
NM_000432.4(MYL2):c.342G>A (p.Leu114=) rs199572927 0.00032
NM_000432.4(MYL2):c.*102C>A rs542961456 0.00029
NM_000432.4(MYL2):c.353+12C>A rs186323458 0.00022
NM_000432.4(MYL2):c.*10C>T rs193922452 0.00007
NM_000432.4(MYL2):c.*29C>T rs371503244 0.00006
NM_000432.4(MYL2):c.275-7G>A rs373241541 0.00006
NM_000432.4(MYL2):c.354-18G>A rs752927354 0.00003
NM_000432.4(MYL2):c.*117A>C rs192821062
NM_000432.4(MYL2):c.*18C>G rs550546518
NM_000432.4(MYL2):c.*53C>G rs1592798356
NM_000432.4(MYL2):c.169+198del rs3216888
NM_000432.4(MYL2):c.170-54T>C rs7980471
NM_000432.4(MYL2):c.274+10del rs2136772075
NM_000432.4(MYL2):c.274+15G>C rs587781090
NM_000432.4(MYL2):c.274+15del rs2136772062
NM_000432.4(MYL2):c.274+16_274+17insTC rs200007468
NM_000432.4(MYL2):c.274+17G>C rs201782797
NM_000432.4(MYL2):c.274+25_274+26insGT rs2136772037
NM_000432.4(MYL2):c.274+27del rs2136772020
NM_000432.4(MYL2):c.274+59del rs971115394
NM_000432.4(MYL2):c.274+8del rs2136772096
NM_000432.4(MYL2):c.274+9GT[10] rs142567411
NM_000432.4(MYL2):c.274+9GT[8] rs142567411
NM_000432.4(MYL2):c.274+9del rs730880939
NM_000432.4(MYL2):c.353+20del rs3833910
NM_000432.4(MYL2):c.353+46dup rs142220381
NM_000432.4(MYL2):c.353+51C>T rs2233260
NM_000432.4(MYL2):c.403-96del rs72145780
NM_000432.4(MYL2):c.93+183_93+186del rs200763840

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