ClinVar Miner

List of variants in gene LIFR reported as likely benign for Stüve-Wiedemann syndrome

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Total variants: 27
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HGVS dbSNP
NM_001127671.2(LIFR):c.*2567G>A rs112458059
NM_001127671.2(LIFR):c.*2570G>C
NM_001127671.2(LIFR):c.*2712C>T rs547688841
NM_001127671.2(LIFR):c.*3851T>A rs78474283
NM_001127671.2(LIFR):c.*398C>G
NM_001127671.2(LIFR):c.*4154A>G
NM_001127671.2(LIFR):c.*5125C>T rs147202739
NM_001127671.2(LIFR):c.*6640dup rs57386567
NM_001127671.2(LIFR):c.1080G>A (p.Ala360=) rs769294023
NM_001127671.2(LIFR):c.1221T>C (p.Asn407=) rs372077841
NM_001127671.2(LIFR):c.147T>G (p.Ala49=) rs879807300
NM_001127671.2(LIFR):c.1722G>A (p.Ser574=) rs200521119
NM_001127671.2(LIFR):c.1937C>A (p.Thr646Asn) rs79040751
NM_001127671.2(LIFR):c.1974C>T (p.Val658=) rs762685098
NM_001127671.2(LIFR):c.2217G>A (p.Ser739=) rs747295716
NM_001127671.2(LIFR):c.2302A>G (p.Arg768Gly) rs139848756
NM_001127671.2(LIFR):c.2447A>G (p.Asp816Gly) rs74856317
NM_001127671.2(LIFR):c.2463G>A (p.Pro821=) rs749085598
NM_001127671.2(LIFR):c.2497+14T>G
NM_001127671.2(LIFR):c.2498-7G>A rs113078097
NM_001127671.2(LIFR):c.2591+6A>T
NM_001127671.2(LIFR):c.2670+6C>G rs898718526
NM_001127671.2(LIFR):c.2934G>A (p.Gln978=) rs148354076
NM_001127671.2(LIFR):c.3060G>A (p.Glu1020=) rs537706381
NM_001127671.2(LIFR):c.3087A>G (p.Arg1029=) rs138418444
NM_001127671.2(LIFR):c.3288C>A (p.Asn1096Lys) rs3729751
NM_001127671.2(LIFR):c.954C>T (p.Thr318=) rs61748202

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