List of variants in gene FAT4 reported as uncertain significance 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: 15

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HGVS	dbSNP
NM_001291303.3(FAT4):c.14311C>T (p.Arg4771Cys)
NM_001291303.3(FAT4):c.9800A>G (p.His3267Arg)	rs773545119
NM_024582.4(FAT4):c.1163C>T (p.Pro388Leu)	rs991371776
NM_024582.4(FAT4):c.12064C>T (p.Arg4022Trp)	rs138019311
NM_024582.4(FAT4):c.13411G>A (p.Val4471Ile)	rs145835705
NM_024582.4(FAT4):c.14660G>A (p.Arg4887Lys)	rs35845544
NM_024582.4(FAT4):c.3328G>A (p.Glu1110Lys)	rs377275274
NM_024582.4(FAT4):c.3424G>A (p.Val1142Met)	rs202188213
NM_024582.4(FAT4):c.3682C>G (p.Gln1228Glu)	rs200227715
NM_024582.4(FAT4):c.5275A>G (p.Ile1759Val)	rs145639192
NM_024582.4(FAT4):c.5987A>G (p.Lys1996Arg)	rs140055438
NM_024582.4(FAT4):c.6094A>G (p.Thr2032Ala)	rs147314754
NM_024582.4(FAT4):c.7261G>A (p.Ala2421Thr)	rs776977766
NM_024582.4(FAT4):c.8072C>T (p.Ser2691Leu)	rs148918820
NM_024582.4(FAT4):c.9596A>G (p.Tyr3199Cys)	rs115895451

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