ClinVar Miner

Variants in gene combination FAT2, SLC36A1 with conflicting interpretations reported as "likely benign and "uncertain significance"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 25
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HGVS dbSNP gnomAD frequency
NM_001447.3(FAT2):c.10666A>G (p.Thr3556Ala) rs200708864 0.00013
NM_001447.3(FAT2):c.7558A>G (p.Ile2520Val) rs371832909 0.00011
NM_001447.3(FAT2):c.10148C>T (p.Ala3383Val)
NM_001447.3(FAT2):c.10413C>A (p.Asn3471Lys)
NM_001447.3(FAT2):c.11375G>A (p.Arg3792Gln)
NM_001447.3(FAT2):c.11452G>A (p.Val3818Ile)
NM_001447.3(FAT2):c.11579T>C (p.Met3860Thr)
NM_001447.3(FAT2):c.12112G>A (p.Glu4038Lys)
NM_001447.3(FAT2):c.3944C>T (p.Thr1315Met)
NM_001447.3(FAT2):c.4280G>A (p.Arg1427His)
NM_001447.3(FAT2):c.4406G>A (p.Arg1469Gln)
NM_001447.3(FAT2):c.4523C>T (p.Thr1508Met)
NM_001447.3(FAT2):c.4750C>T (p.Arg1584Trp)
NM_001447.3(FAT2):c.4907G>T (p.Gly1636Val)
NM_001447.3(FAT2):c.5477C>T (p.Ser1826Leu)
NM_001447.3(FAT2):c.5512T>C (p.Phe1838Leu)
NM_001447.3(FAT2):c.5629T>C (p.Tyr1877His)
NM_001447.3(FAT2):c.6974A>G (p.Asn2325Ser)
NM_001447.3(FAT2):c.8000G>C (p.Gly2667Ala)
NM_001447.3(FAT2):c.8183G>A (p.Arg2728Gln)
NM_001447.3(FAT2):c.8517C>A (p.Asp2839Glu)
NM_001447.3(FAT2):c.8558A>G (p.Glu2853Gly)
NM_001447.3(FAT2):c.9434A>G (p.Asn3145Ser)
NM_001447.3(FAT2):c.9701G>A (p.Gly3234Asp)
NM_001447.3(FAT2):c.9910G>A (p.Val3304Met)

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