ClinVar Miner

List of variants in gene LRSAM1 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 65
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HGVS dbSNP gnomAD frequency
NM_001005373.4(LRSAM1):c.620-296C>T rs79075038 0.03777
NM_001005373.4(LRSAM1):c.903+93A>G rs56131876 0.02821
NM_001005373.4(LRSAM1):c.904-67C>T rs56160932 0.02702
NM_001005373.4(LRSAM1):c.1699-168G>A rs76576041 0.01485
NM_001005373.4(LRSAM1):c.252+51G>A rs142333739 0.01473
NM_001005373.4(LRSAM1):c.-33+445G>T rs141227166 0.01469
NM_001005373.4(LRSAM1):c.129+128C>T rs113996142 0.01469
NM_001005373.4(LRSAM1):c.1600-152G>A rs142343329 0.01123
NM_001005373.4(LRSAM1):c.252+134T>C rs145947414 0.01040
NM_001005373.4(LRSAM1):c.253-98G>A rs115106486 0.00910
NM_001005373.4(LRSAM1):c.1422+129C>T rs113022868 0.00866
NM_001005373.4(LRSAM1):c.1831-58A>G rs185352597 0.00831
NM_001005373.4(LRSAM1):c.904-48G>A rs143901401 0.00802
NM_001005373.4(LRSAM1):c.1831-66C>T rs137858765 0.00800
NM_001005373.4(LRSAM1):c.529-246C>T rs190101207 0.00798
NM_001005373.4(LRSAM1):c.1913-167_1913-163del rs202170304 0.00768
NM_001005373.4(LRSAM1):c.322-51G>A rs182192023 0.00619
NM_001005373.4(LRSAM1):c.750+313G>A rs184257921 0.00383
NM_001005373.4(LRSAM1):c.1044-313G>A rs183022187 0.00380
NM_001005373.4(LRSAM1):c.1600-140C>T rs370404396 0.00344
NM_001005373.4(LRSAM1):c.1975G>A (p.Val659Met) rs140786088 0.00342
NM_001005373.4(LRSAM1):c.965A>G (p.Gln322Arg) rs56380300 0.00328
NM_001005373.4(LRSAM1):c.72+45C>T rs74876850 0.00321
NM_001005373.4(LRSAM1):c.1830+36C>T rs3802361 0.00149
NM_001005373.4(LRSAM1):c.268G>A (p.Asp90Asn) rs117692127 0.00133
NM_001005373.4(LRSAM1):c.406+23C>T rs117197911 0.00129
NM_001005373.4(LRSAM1):c.1974T>C (p.Ser658=) rs140336379 0.00065
NM_001005373.4(LRSAM1):c.406+15G>T rs201808404 0.00064
NM_001005373.4(LRSAM1):c.407-35T>G rs141724747 0.00063
NM_001005373.4(LRSAM1):c.1860C>T (p.His620=) rs147734401 0.00054
NM_001005373.4(LRSAM1):c.1225C>G (p.Gln409Glu) rs149540339 0.00039
NM_001005373.4(LRSAM1):c.2111G>A (p.Arg704His) rs140808447 0.00035
NM_001005373.4(LRSAM1):c.1950G>A (p.Thr650=) rs199887448 0.00029
NM_001005373.4(LRSAM1):c.2139C>T (p.Ile713=) rs373990000 0.00024
NM_001005373.4(LRSAM1):c.569G>A (p.Arg190Gln) rs142782210 0.00020
NM_001005373.4(LRSAM1):c.94G>A (p.Asp32Asn) rs150784835 0.00017
NM_001005373.4(LRSAM1):c.1199G>A (p.Arg400Gln) rs150344223 0.00014
NM_001005373.4(LRSAM1):c.1046A>G (p.Gln349Arg) rs200595164 0.00011
NM_001005373.4(LRSAM1):c.1405C>T (p.Arg469Trp) rs376468970 0.00011
NM_001005373.4(LRSAM1):c.751-8C>G rs367823841 0.00011
NM_001005373.4(LRSAM1):c.993G>A (p.Thr331=) rs368674859 0.00009
NM_001005373.4(LRSAM1):c.1026G>T (p.Leu342=) rs367599324 0.00008
NM_001005373.4(LRSAM1):c.1027C>T (p.Leu343=) rs369353985 0.00008
NM_001005373.4(LRSAM1):c.339G>A (p.Arg113=) rs146613642 0.00007
NM_001005373.4(LRSAM1):c.*5T>A rs1447674725 0.00004
NM_001005373.4(LRSAM1):c.1382A>T (p.Gln461Leu) rs145382004 0.00004
NM_001005373.4(LRSAM1):c.1514C>T (p.Ser505Leu) rs146106537 0.00004
NM_001005373.4(LRSAM1):c.392C>T (p.Thr131Ile) rs772202137 0.00004
NM_001005373.4(LRSAM1):c.1043+5G>A rs780868977 0.00002
NM_001005373.4(LRSAM1):c.102C>T (p.Leu34=) rs762785076 0.00001
NM_001005373.4(LRSAM1):c.362G>A (p.Arg121His) rs143910539 0.00001
NM_001005373.4(LRSAM1):c.513C>T (p.His171=) rs757426906 0.00001
NM_001005373.4(LRSAM1):c.1043+104C>T rs142195263
NM_001005373.4(LRSAM1):c.1088+44del rs371152397
NM_001005373.4(LRSAM1):c.1203C>T (p.Leu401=) rs774735924
NM_001005373.4(LRSAM1):c.129+195dup
NM_001005373.4(LRSAM1):c.153A>G (p.Thr51=)
NM_001005373.4(LRSAM1):c.1629G>A (p.Arg543=) rs752477588
NM_001005373.4(LRSAM1):c.1698A>G (p.Gln566=) rs1256215388
NM_001005373.4(LRSAM1):c.1707G>T (p.Gly569=)
NM_001005373.4(LRSAM1):c.1953C>A (p.Ala651=)
NM_001005373.4(LRSAM1):c.30C>T (p.Pro10=) rs1588090324
NM_001005373.4(LRSAM1):c.321+162_321+163dup rs373307015
NM_001005373.4(LRSAM1):c.321+163del rs373307015
NM_001005373.4(LRSAM1):c.620-9C>G rs1588114537

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