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Links from Gene

Items: 15

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FNDC1, FNDC1-AS1
(A11G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129997480, LOC129997522
+288 more
Deletion
Chromosome 6q24-q25 deletion syndrome
GPathogenic
FNDC1, FNDC1-AS1
(S36T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FNDC1, FNDC1-AS1
(A34E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FNDC1, FNDC1-AS1
(V29F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACAT2, AIRN
+115 more
Copy number gain
See cases
GUncertain significance
LOC129997450, LOC129997451
+1002 more
Copy number gain
See cases
GPathogenic
LOC101929460, LOC102724087
+572 more
Copy number gain
See cases
GPathogenic
LOC129997640, LOC129997641
+564 more
Copy number loss
See cases
GPathogenic
AKAP12, ARID1B
+288 more
Copy number loss
See cases
GPathogenic
SOD2, SOD2-OT1
+270 more
Copy number loss
See cases
GPathogenic
IGF2R, KIF25
+540 more
Copy number loss
See cases
GPathogenic
ACAT2, AFDN
+549 more
Copy number loss
See cases
GPathogenic
DYNLT1, EZR
+100 more
Copy number gain
See cases
GPathogenic
LOC129389719, LOC129389720
+866 more
Copy number gain
See cases
GPathogenic
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