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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RAD50, TH2-LCR
+1 more
(M1140I)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
TH2LCRR, RAD50
+1 more
(R1180Q)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
TH2LCRR, RAD50
+1 more
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
RAD50, TH2LCRR
Single nucleotide variant
(synonymous variant +1 more)
not specified
+4 more
GBenign
RAD50, TH2LCRR
(S1297L)
Single nucleotide variant
(missense variant)
Familial cancer of breast
GUncertain significance
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