List of variants in gene combination FANCF, LOC130005443 reported by Sema4, Sema4

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_022725.4(FANCF):c.959C>T (p.Pro320Leu)	rs45451294	0.01158
NM_022725.4(FANCF):c.1012G>A (p.Asp338Asn)	rs149687560	0.00003
NM_022725.4(FANCF):c.1056A>C (p.Leu352Phe)	rs754545069	0.00001
NM_022725.4(FANCF):c.993C>G (p.Thr331=)	rs751274756	0.00001
NM_022725.4(FANCF):c.1001C>T (p.Ala334Val)	rs772941983
NM_022725.4(FANCF):c.1020A>G (p.Glu340=)	rs1858615686

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