List of variants in gene combination FANCD2, LOC107303338 reported as not provided for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_001018115.3(FANCD2):c.2141C>T (p.Pro714Leu)	rs3864017	0.19295
NM_001018115.3(FANCD2):c.1367T>G (p.Leu456Arg)	rs35782247	0.02918
NM_001018115.3(FANCD2):c.1868A>C (p.Gln623Pro)	rs36070315	0.02463
NM_001018115.3(FANCD2):c.2702G>T (p.Gly901Val)	rs35495399	0.02285
NM_001018115.3(FANCD2):c.516A>G (p.Ile172Met)	rs35173688	0.02009
NM_001018115.3(FANCD2):c.195G>C (p.Gln65His)	rs36084488	0.00738
NM_001018115.3(FANCD2):c.1634A>G (p.Asn545Ser)	rs145522204	0.00460
NM_001018115.3(FANCD2):c.983G>A (p.Arg328Gln)	rs35625434	0.00124
NM_001018115.3(FANCD2):c.1777C>T (p.Pro593Ser)	rs147523071	0.00071
NM_001018115.3(FANCD2):c.577A>G (p.Thr193Ala)	rs34936017	0.00070
NM_001018115.3(FANCD2):c.2965C>G (p.Pro989Ala)	rs200568638	0.00003
NM_001018115.3(FANCD2):c.2567C>G (p.Thr856Ser)	rs587778329	0.00001
NM_001018115.3(FANCD2):c.2555C>T (p.Pro852Leu)	rs375827113

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