ClinVar Miner

List of variants in gene SDHAF2 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (1030):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 26
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HGVS dbSNP
NM_017841.2(SDHAF2):c.*12C>T rs113652589
NM_017841.2(SDHAF2):c.153T>G (p.Pro51=) rs769950627
NM_017841.2(SDHAF2):c.156G>A (p.Leu52=) rs773466310
NM_017841.2(SDHAF2):c.15A>G (p.Thr5=) rs144511254
NM_017841.2(SDHAF2):c.21C>T (p.Phe7=) rs892955355
NM_017841.2(SDHAF2):c.240G>A (p.Leu80=) rs1223446048
NM_017841.2(SDHAF2):c.24G>A (p.Ser8=) rs764251580
NM_017841.2(SDHAF2):c.264T>G (p.Leu88=) rs1554984669
NM_017841.2(SDHAF2):c.294A>G (p.Thr98=) rs762441285
NM_017841.2(SDHAF2):c.319C>T (p.Arg107Cys) rs140191819
NM_017841.2(SDHAF2):c.320G>A (p.Arg107His) rs535627239
NM_017841.2(SDHAF2):c.327T>A (p.Ile109=) rs757670376
NM_017841.2(SDHAF2):c.32C>T (p.Ser11Leu) rs148425779
NM_017841.2(SDHAF2):c.360C>T (p.Tyr120=) rs1328610836
NM_017841.2(SDHAF2):c.37-7A>G rs1554984610
NM_017841.2(SDHAF2):c.370+8G>C rs764742919
NM_017841.2(SDHAF2):c.453G>A (p.Gln151=) rs1271900425
NM_017841.2(SDHAF2):c.465C>T (p.Ala155=) rs758154733
NM_017841.2(SDHAF2):c.6G>A (p.Ala2=) rs747571875
NM_017841.2(SDHAF2):c.6G>T (p.Ala2=) rs747571875
NM_017841.2(SDHAF2):c.97C>T (p.Arg33Cys) rs144867876
NM_017841.4(SDHAF2):c.260+10T>C rs1590764949
NM_017841.4(SDHAF2):c.269C>T (p.Ala90Val) rs373951663
NM_017841.4(SDHAF2):c.321C>T (p.Arg107=) rs754291669
NM_017841.4(SDHAF2):c.370+7G>C rs1590765180
NM_017841.4(SDHAF2):c.387A>G (p.Pro129=) rs770383127

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