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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 38

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HGVS	dbSNP	gnomAD frequency
NM_001018115.3(FANCD2):c.1414-23T>C	rs10222446	0.48329
NM_001018115.3(FANCD2):c.784-19C>T	rs9879080	0.23357
NM_001018115.3(FANCD2):c.2976+36T>C	rs6805869	0.23353
NM_001018115.3(FANCD2):c.990-38C>G	rs9809061	0.22591
NM_001018115.3(FANCD2):c.695+16G>C	rs17032283	0.20237
NM_001018115.3(FANCD2):c.696-138C>T	rs35220123	0.20233
NM_001018115.3(FANCD2):c.439-16A>G	rs17032278	0.20185
NM_001018115.3(FANCD2):c.1122A>G (p.Val374=)	rs34046352	0.19892
NM_001018115.3(FANCD2):c.2270-28G>T	rs34608006	0.19876
NM_001018115.3(FANCD2):c.2141C>T (p.Pro714Leu)	rs3864017	0.19295
NM_001018115.3(FANCD2):c.1413+38A>C	rs7615646	0.10867
NM_001018115.3(FANCD2):c.2269+37A>G	rs34323624	0.03335
NM_001018115.3(FANCD2):c.2712C>T (p.Asn904=)	rs35594075	0.03203
NM_001018115.3(FANCD2):c.571-31G>A	rs35749514	0.03113
NM_001018115.3(FANCD2):c.1509C>T (p.Asn503=)	rs6785756	0.03005
NM_001018115.3(FANCD2):c.1367T>G (p.Leu456Arg)	rs35782247	0.02918
NM_001018115.3(FANCD2):c.2124T>C (p.Phe708=)	rs9809716	0.02768
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.2148C>G (p.Thr716=)	rs55856815	0.00952
NM_001018115.3(FANCD2):c.2484G>A (p.Lys828=)	rs55980657	0.00869
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.1156T>G (p.Phe386Val)	rs149125003	0.00450
NM_001018115.3(FANCD2):c.1336C>G (p.Leu446Val)	rs34557223	0.00316
NM_001018115.3(FANCD2):c.983G>A (p.Arg328Gln)	rs35625434	0.00124
NM_001018115.3(FANCD2):c.491+10G>A	rs17032279	0.00103
NM_001018115.3(FANCD2):c.205+9T>G	rs34113138	0.00056
NM_001018115.3(FANCD2):c.1170C>T (p.Ser390=)	rs112887807
NM_001018115.3(FANCD2):c.1179T>C (p.Thr393=)	rs72492998
NM_001018115.3(FANCD2):c.1275C>T (p.Tyr425=)	rs764447374
NM_001018115.3(FANCD2):c.1278+3_1278+6del	rs369823368
NM_001018115.3(FANCD2):c.1278+5G>T	rs796652647
NM_001018115.3(FANCD2):c.1401G>A (p.Thr467=)	rs12330369
NM_001018115.3(FANCD2):c.1413+3A>G	rs62245508
NM_001018115.3(FANCD2):c.1414-9C>T	rs35557429
NM_001018115.3(FANCD2):c.2022-5C>T	rs4019784

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