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Links from MedGen

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HABP2
(G481V +1 more)
Single nucleotide variant
(missense variant)
Thyroid cancer, nonmedullary, 5
GUncertain significance
HABP2
Single nucleotide variant
(synonymous variant)
Thyroid cancer, nonmedullary, 5
GUncertain significance
HABP2
(R96W +1 more)
Single nucleotide variant
(missense variant)
Thyroid cancer, nonmedullary, 5
+2 more
GBenign/Likely benign
HABP2
(G316E +1 more)
Single nucleotide variant
(missense variant)
Factor VII Marburg I Variant Thrombophilia
+3 more
GBenign/Likely benign
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