ClinVar Miner

List of variants in gene FMN2 reported as uncertain significance for autosomal recessive disease

Included ClinVar conditions (1198):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_020066.5(FMN2):c.4619C>T (p.Ser1540Leu) rs150801382 0.00221
NM_020066.5(FMN2):c.575A>T (p.Gln192Leu) rs150505248 0.00044
NM_020066.5(FMN2):c.2200C>T (p.Arg734Trp) rs145706266 0.00020
NM_020066.5(FMN2):c.2297G>A (p.Arg766His) rs554313620 0.00011
NM_020066.5(FMN2):c.3560C>T (p.Pro1187Leu) rs372947608 0.00006
NM_020066.5(FMN2):c.2753C>T (p.Ala918Val) rs768693892 0.00005
NM_020066.5(FMN2):c.2240C>T (p.Ser747Phe) rs776610158 0.00001
NM_020066.5(FMN2):c.4865T>C (p.Ile1622Thr) rs1298917573 0.00001
NM_020066.5(FMN2):c.629A>G (p.Gln210Arg) rs1458799973 0.00001
NM_020066.5(FMN2):c.1054G>T (p.Asp352Tyr)
NM_020066.5(FMN2):c.1244C>T (p.Thr415Ile) rs200347646
NM_020066.5(FMN2):c.1378G>A (p.Ala460Thr) rs1463766241
NM_020066.5(FMN2):c.1748A>C (p.Asn583Thr)
NM_020066.5(FMN2):c.2806C>G (p.Pro936Ala)
NM_020066.5(FMN2):c.2842_2873del (p.Leu948fs)
NM_020066.5(FMN2):c.3131C>T (p.Pro1044Leu) rs202165125
NM_020066.5(FMN2):c.3230C>T (p.Pro1077Leu)
NM_020066.5(FMN2):c.4468G>T (p.Val1490Phe)
NM_020066.5(FMN2):c.4666C>G (p.Leu1556Val)
NM_020066.5(FMN2):c.884C>T (p.Ser295Phe)

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