ClinVar Miner

List of variants in gene SCN1B reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_001037.5(SCN1B):c.448+181T>C rs55742440 0.42428
NM_001037.5(SCN1B):c.41-313T>A rs8100085 0.41634
NM_001037.5(SCN1B):c.448+610T>C rs67777826 0.28960
NM_001037.5(SCN1B):c.448+679A>C rs61377791 0.28334
NM_001037.5(SCN1B):c.40+15G>T rs72556351 0.19938
NM_001037.5(SCN1B):c.*86A>C rs2278996 0.14285
NM_001037.5(SCN1B):c.*42T>C rs2278995 0.14069
NM_001037.5(SCN1B):c.448+296C>A rs67701503 0.13979
NM_001037.5(SCN1B):c.208-94T>G rs58899423 0.08727
NM_001037.5(SCN1B):c.208-121T>A rs58803373 0.08726
NM_001037.5(SCN1B):c.*6-11C>G rs28365105 0.05977
NM_001037.5(SCN1B):c.449-229C>T rs7256501 0.03134
NM_001037.5(SCN1B):c.207+14G>A rs16969924 0.02860
NM_001037.5(SCN1B):c.41-239T>G rs73929262 0.02601
NM_001037.5(SCN1B):c.591-150A>G rs61457558 0.02240
NM_001037.5(SCN1B):c.208-320T>C rs56158208 0.02189
NM_001037.5(SCN1B):c.449-25C>T rs72550246 0.01950
NM_001037.5(SCN1B):c.501T>C (p.Ile167=) rs16969930 0.01942
NM_001037.5(SCN1B):c.591-14C>A rs28365109 0.00920
NM_001037.5(SCN1B):c.-9C>A rs66671189 0.00603
NM_001037.5(SCN1B):c.300C>T (p.Asp100=) rs16969927 0.00539
NM_001037.5(SCN1B):c.*5+31G>A rs28365108 0.00361
NM_001037.5(SCN1B):c.28G>A (p.Gly10Ser) rs72552027 0.00249
NM_001037.5(SCN1B):c.267C>T (p.Arg89=) rs140949982 0.00232
NM_001037.5(SCN1B):c.448+193G>A rs66876876 0.00227
NM_001037.5(SCN1B):c.448+321G>A rs72558028 0.00173
NM_001037.5(SCN1B):c.448+29C>T rs186759145 0.00163
NM_001037.5(SCN1B):c.588T>C (p.Asn196=) rs77244433 0.00117
NM_001037.5(SCN1B):c.5+7C>T rs28365106 0.00091
NM_001037.5(SCN1B):c.351C>T (p.Gly117=) rs3746255 0.00082
NM_001037.5(SCN1B):c.207+34A>C rs369688072 0.00059
NM_001037.5(SCN1B):c.412G>A (p.Val138Ile) rs72558029 0.00058
NM_001037.5(SCN1B):c.448+112G>A rs72558026 0.00049
NM_001037.5(SCN1B):c.448+314C>A rs373295182 0.00043
NM_001037.5(SCN1B):c.590+16G>A rs201053958 0.00036
NM_001037.5(SCN1B):c.448+320C>T rs570257058 0.00033
NM_001037.5(SCN1B):c.448+444G>A rs375266320 0.00023
NM_001037.5(SCN1B):c.348G>A (p.Ser116=) rs375050816 0.00021
NM_001037.5(SCN1B):c.632G>A (p.Cys211Tyr) rs150721582 0.00021
NM_001037.5(SCN1B):c.207+7G>A rs374588869 0.00016
NM_001037.5(SCN1B):c.-27G>C rs758958222 0.00013
NM_001037.5(SCN1B):c.-40C>G rs587781150 0.00007
NM_001037.5(SCN1B):c.448+8G>C rs200222933 0.00006
NM_001037.5(SCN1B):c.561C>T (p.Ala187=) rs587781152 0.00005
NM_001037.5(SCN1B):c.208-14C>T rs72550272 0.00004
NM_001037.5(SCN1B):c.448+299A>G rs1027861663 0.00004
NM_001037.5(SCN1B):c.448+48A>C rs757515975 0.00004
NM_001037.5(SCN1B):c.63C>T (p.Cys21=) rs200339565 0.00002
NM_001037.5(SCN1B):c.448+230C>T rs769132369 0.00001
NM_001037.5(SCN1B):c.448+346G>A rs76302703 0.00001
NC_000019.10:g.35030440CGC[10] rs557140301
NM_001037.5(SCN1B):c.*527T>C rs41275828
NM_001037.5(SCN1B):c.*57del rs2151749193
NM_001037.5(SCN1B):c.207+19C>T rs201872896
NM_001037.5(SCN1B):c.208-189G>A rs56276191
NM_001037.5(SCN1B):c.40+6T>C rs587781151
NM_001037.5(SCN1B):c.448+301G>A rs67486287
NM_001037.5(SCN1B):c.448+337G>A rs369032304
NM_001037.5(SCN1B):c.492T>C (p.Tyr164=) rs535042320
NM_001037.5(SCN1B):c.591-22A>T rs200116490
NM_199037.3(SCN1B):c.749G>C (p.Arg250Thr) rs67486287

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