ClinVar Miner

List of variants in gene combination LHCGR, STON1-GTF2A1L reported as likely benign

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Total variants: 60
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HGVS dbSNP gnomAD frequency
NM_000233.4(LHCGR):c.866+25C>T rs147917820 0.01273
NM_000233.4(LHCGR):c.610C>T (p.Leu204=) rs61996322 0.01070
NM_000233.4(LHCGR):c.*131C>T rs73928204 0.00766
NM_000233.4(LHCGR):c.1010T>C (p.Leu337Ser) rs61996314 0.00677
NM_000233.4(LHCGR):c.622G>A (p.Val208Ile) rs61996321 0.00614
NM_000233.4(LHCGR):c.309-55T>C rs143404304 0.00531
NM_000233.4(LHCGR):c.606-5C>T rs78135094 0.00283
NM_000233.4(LHCGR):c.867-176A>C rs113455986 0.00272
NM_000233.4(LHCGR):c.458+3A>G rs76210637 0.00251
NM_000233.4(LHCGR):c.*535G>A rs534109670 0.00191
NM_000233.4(LHCGR):c.568C>A (p.Gln190Lys) rs61996318 0.00163
NM_000233.4(LHCGR):c.*22T>G rs192235905 0.00139
NM_000233.4(LHCGR):c.1360G>A (p.Val454Ile) rs114320052 0.00116
NM_000233.4(LHCGR):c.*577T>A rs542577446 0.00098
NM_000233.4(LHCGR):c.430G>A (p.Val144Ile) rs121912539 0.00035
NM_000233.4(LHCGR):c.161+9A>G rs573699597 0.00031
NM_000233.4(LHCGR):c.1916G>A (p.Ser639Asn) rs149766676 0.00027
NM_000233.4(LHCGR):c.561A>G (p.Glu187=) rs369601921 0.00027
NM_000233.4(LHCGR):c.*7C>T rs200256443 0.00026
NM_000233.4(LHCGR):c.1797C>A (p.Ile599=) rs143697410 0.00024
NM_000233.4(LHCGR):c.426G>A (p.Thr142=) rs142554296 0.00019
NM_000233.4(LHCGR):c.378A>C (p.Lys126Asn) rs373456950 0.00015
NM_000233.4(LHCGR):c.672G>A (p.Pro224=) rs267599401 0.00015
NM_000233.4(LHCGR):c.54G>A (p.Gln18=) rs780848944 0.00013
NM_000233.4(LHCGR):c.309-17T>C rs549649504 0.00009
NM_000233.4(LHCGR):c.1169A>G (p.Lys390Arg) rs549696399 0.00008
NM_000233.4(LHCGR):c.680+9A>G rs766301939 0.00008
NM_000233.4(LHCGR):c.1669G>A (p.Glu557Lys) rs146785679 0.00005
NM_000233.4(LHCGR):c.1875A>T (p.Ile625=) rs200691173 0.00005
NM_000233.4(LHCGR):c.1025G>A (p.Arg342Gln) rs149957775 0.00003
NM_000233.4(LHCGR):c.161+8C>T rs544275678 0.00003
NM_000233.4(LHCGR):c.1752T>C (p.Pro584=) rs377665383 0.00003
NM_000233.4(LHCGR):c.2002A>C (p.Thr668Pro) rs199807908 0.00003
NM_000233.4(LHCGR):c.207C>T (p.Phe69=) rs911406588 0.00003
NM_001198593.2(STON1-GTF2A1L):c.3442-20603G>A rs779799454 0.00003
NM_000233.4(LHCGR):c.1971A>G (p.Ser657=) rs764444931 0.00002
NM_000233.4(LHCGR):c.233+14T>C rs758708866 0.00002
NM_000233.4(LHCGR):c.605+8T>C rs1553392347 0.00002
NM_000233.4(LHCGR):c.628C>T (p.Leu210=) rs368171908 0.00002
NM_000233.4(LHCGR):c.81G>A (p.Glu27=) rs527550554 0.00002
NM_000233.4(LHCGR):c.1095G>T (p.Leu365=) rs74447072 0.00001
NM_000233.4(LHCGR):c.1374C>T (p.Thr458=) rs776179025 0.00001
NM_000233.4(LHCGR):c.2091A>T (p.Thr697=) rs148244033 0.00001
NM_000233.4(LHCGR):c.2095T>A (p.Cys699Ser) rs778585416 0.00001
NM_000233.4(LHCGR):c.264G>A (p.Arg88=) rs141473843 0.00001
NM_000233.4(LHCGR):c.309-20T>G rs1300001270 0.00001
NM_000233.4(LHCGR):c.*281del rs558291070
NM_000233.4(LHCGR):c.*53dup rs200887026
NM_000233.4(LHCGR):c.1023C>T (p.Pro341=) rs2529702630
NM_000233.4(LHCGR):c.1095G>A (p.Leu365=) rs74447072
NM_000233.4(LHCGR):c.111G>A (p.Val37=)
NM_000233.4(LHCGR):c.1590C>A (p.Thr530=) rs1331743516
NM_000233.4(LHCGR):c.308+11G>A
NM_000233.4(LHCGR):c.337T>A (p.Tyr113Asn) rs140691492
NM_000233.4(LHCGR):c.383+15T>C rs1186300707
NM_000233.4(LHCGR):c.605+9T>G rs1572851553
NM_000233.4(LHCGR):c.606-268G>A rs111338389
NM_000233.4(LHCGR):c.681-16C>T
NM_000233.4(LHCGR):c.947+968_947+970del rs539220717
NM_000233.4(LHCGR):c.978G>C (p.Leu326=)

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