ClinVar Miner

List of variants in gene combination FANCD2, LOC107303338 reported as benign for abdominal and pelvic region disorder

Included ClinVar conditions (956):
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Gene type:
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Total variants: 17
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HGVS dbSNP
NM_033084.5(FANCD2):c.1122A>G (p.Val374=) rs34046352
NM_033084.5(FANCD2):c.1137G>T (p.Val379=) rs72492997
NM_033084.5(FANCD2):c.1170C>T (p.Ser390=) rs112887807
NM_033084.5(FANCD2):c.1179T>C (p.Thr393=) rs72492998
NM_033084.5(FANCD2):c.1214A>G (p.Asn405Ser) rs73126218
NM_033084.5(FANCD2):c.1278+3_1278+5del rs375350046
NM_033084.5(FANCD2):c.1401G>A (p.Thr467=) rs12330369
NM_033084.5(FANCD2):c.1413+14T>C rs12330599
NM_033084.5(FANCD2):c.1413+3A>G rs62245508
NM_033084.5(FANCD2):c.2141C>T (p.Pro714Leu) rs3864017
NM_033084.5(FANCD2):c.2702G>T (p.Gly901Val) rs35495399
NM_033084.5(FANCD2):c.2877A>G (p.Gln959=) rs145953386
NM_033084.5(FANCD2):c.378-6_378-5del rs55973240
NM_033084.6(FANCD2):c.1135-25G>A
NM_033084.6(FANCD2):c.2494+95C>A
NM_033084.6(FANCD2):c.2494+97T>A
NM_033084.6(FANCD2):c.2494+98C>A

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