ClinVar Miner

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

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 21
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HGVS dbSNP gnomAD frequency
NM_001447.3(FAT2):c.4524G>A (p.Thr1508=) rs35489594 0.00541
NM_001447.3(FAT2):c.11989G>A (p.Glu3997Lys) rs146458760 0.00444
NM_001447.3(FAT2):c.9642C>T (p.Tyr3214=) rs143792947 0.00372
NM_001447.3(FAT2):c.9930C>T (p.Asn3310=) rs73272071 0.00260
NM_001447.3(FAT2):c.3976C>T (p.Leu1326Phe) rs146280178 0.00247
NM_001447.3(FAT2):c.5726C>T (p.Thr1909Ile) rs142001888 0.00215
NM_001447.3(FAT2):c.9010G>A (p.Val3004Ile) rs142809371 0.00128
NM_001447.3(FAT2):c.8206A>G (p.Lys2736Glu) rs570674049 0.00047
NM_001447.3(FAT2):c.12464C>G (p.Ser4155Cys) rs145466001 0.00031
NM_001447.3(FAT2):c.10148C>T (p.Ala3383Val)
NM_001447.3(FAT2):c.4405C>A (p.Arg1469=)
NM_001447.3(FAT2):c.4537G>A (p.Asp1513Asn) rs61743237
NM_001447.3(FAT2):c.4614C>T (p.Phe1538=)
NM_001447.3(FAT2):c.5477C>T (p.Ser1826Leu)
NM_001447.3(FAT2):c.5720T>C (p.Ile1907Thr)
NM_001447.3(FAT2):c.6149G>A (p.Arg2050Gln)
NM_001447.3(FAT2):c.6449C>T (p.Thr2150Met)
NM_001447.3(FAT2):c.7527T>C (p.Asp2509=)
NM_001447.3(FAT2):c.8608A>G (p.Thr2870Ala)
NM_001447.3(FAT2):c.8707G>C (p.Ala2903Pro)
NM_001447.3(FAT2):c.8714G>A (p.Arg2905Gln)

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