List of variants in gene combination FANCF, LOC130005443 reported as likely benign for immune system disorder

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_022725.4(FANCF):c.1054T>C (p.Leu352=)	rs61752917	0.00011
NM_022725.4(FANCF):c.1002G>C (p.Ala334=)	rs761698961	0.00003
NM_022725.4(FANCF):c.1026T>C (p.Pro342=)	rs745879868	0.00001
NM_022725.4(FANCF):c.984C>T (p.Ala328=)	rs1858616188	0.00001
NM_022725.4(FANCF):c.993C>G (p.Thr331=)	rs751274756	0.00001
NM_022725.4(FANCF):c.1020A>G (p.Glu340=)	rs1858615686
NM_022725.4(FANCF):c.1035C>T (p.Ser345=)	rs1554963603
NM_022725.4(FANCF):c.1038C>T (p.Ile346=)
NM_022725.4(FANCF):c.1044A>G (p.Thr348=)	rs2133796228
NM_022725.4(FANCF):c.987G>C (p.Leu329=)	rs2133796354
NM_022725.4(FANCF):c.993C>A (p.Thr331=)

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