ClinVar Miner

List of variants in gene MTHFR reported as benign for not provided

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Gene type:
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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_005957.5(MTHFR):c.1752+146T>C rs7518348 0.90139
NM_005957.5(MTHFR):c.476-304A>G rs7533315 0.74629
NM_005957.5(MTHFR):c.586+149A>G rs11121832 0.74621
NM_005957.5(MTHFR):c.1166+31C>T rs1994798 0.55967
NM_005957.5(MTHFR):c.1286A>C (p.Glu429Ala) rs1801131 0.25830
NM_005957.5(MTHFR):c.1753-48C>G rs3818762 0.22829
NM_005957.5(MTHFR):c.1632+35G>A rs1476413 0.22803
NM_005957.5(MTHFR):c.1167-76G>T rs12121543 0.20910
NM_005957.5(MTHFR):c.236+160T>C rs17367504 0.13468
NM_005957.5(MTHFR):c.1632+225G>A rs13306556 0.10272
NM_005957.5(MTHFR):c.586+152T>C rs13306553 0.09780
NM_005957.5(MTHFR):c.1531-80G>A rs17375901 0.04653
NM_005957.5(MTHFR):c.780+179C>T rs45439601 0.04558
NM_005957.5(MTHFR):c.1752+45G>A rs45529133 0.04266
NM_005957.5(MTHFR):c.1781G>A (p.Arg594Gln) rs2274976 0.03996
NM_005957.5(MTHFR):c.1752+79G>A rs55686944 0.03554
NM_005957.5(MTHFR):c.1031+117G>A rs2066465 0.03133
NM_005957.5(MTHFR):c.1632+94G>C rs45578836 0.03124
NM_005957.5(MTHFR):c.-13-91C>T rs17037404 0.02827
NM_005957.5(MTHFR):c.476-76G>A rs2066469 0.01897
NM_005957.5(MTHFR):c.1958C>T (p.Thr653Met) rs35737219 0.01462
NM_005957.5(MTHFR):c.1476G>A (p.Pro492=) rs35653697 0.00937
NM_005957.5(MTHFR):c.236+170dup rs55645287
NM_005957.5(MTHFR):c.476-79G>A rs2066471

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