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Links from MedGen

Items: 1 to 100 of 1130

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SDHB
(D48fs)
Duplication
(frameshift variant)
Pheochromocytoma
+2 more
GPathogenic
SDHB
(R91T)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
Single nucleotide variant
(synonymous variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
(A52S)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(I248N +1 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(K78M)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(A43V)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+3 more
GUncertain significance
SDHB
Single nucleotide variant
(synonymous variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
(M58I)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(W200C +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
SDHB
Single nucleotide variant
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
Single nucleotide variant
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
(K167R +1 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(A244fs +1 more)
Deletion
(frameshift variant)
Pheochromocytoma
+2 more
GPathogenic
SDHB
Single nucleotide variant
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
(P129T)
Single nucleotide variant
(missense variant +1 more)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(P49fs)
Deletion
(frameshift variant)
Pheochromocytoma
+2 more
GPathogenic
SDHB
(D224N +1 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
Single nucleotide variant
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
(R233fs +1 more)
Deletion
(frameshift variant)
Pheochromocytoma
+2 more
GPathogenic
SDHB
Single nucleotide variant
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
Single nucleotide variant
(splice acceptor variant)
Pheochromocytoma
+2 more
GPathogenic
SDHB
Single nucleotide variant
(synonymous variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
(P49Q)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
Single nucleotide variant
(synonymous variant)
Pheochromocytoma
+2 more
GLikely benign
LOC129929542, SDHB
Single nucleotide variant
(synonymous variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
(G96R)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(K137N)
Single nucleotide variant
(missense variant +1 more)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(P236R +1 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(I79T)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(K160E +1 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(R94I)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(K151R +1 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
Insertion
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
Deletion
(splice acceptor variant)
Pheochromocytoma
+2 more
GLikely pathogenic
SDHB
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+3 more
GLikely benign
SDHB
(E95Q)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(R91S)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
Single nucleotide variant
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
LOC129929541, SDHB
Single nucleotide variant
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
(M213R +1 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(I263T +1 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
LOC129929542, SDHB
Single nucleotide variant
(synonymous variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
(F238V +1 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
Single nucleotide variant
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
(E158K +1 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(R27P)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
Single nucleotide variant
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
(C168R +1 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(E257V +1 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(Y152fs +1 more)
Duplication
(frameshift variant)
Pheochromocytoma
+2 more
GPathogenic
SDHB
(S222P +1 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
Single nucleotide variant
(synonymous variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
Single nucleotide variant
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
(G166R +1 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(W182G +1 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
Microsatellite
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
Single nucleotide variant
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
LOC129929542, SDHB
Single nucleotide variant
(intron variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(E257A +1 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(K41del)
Deletion
(inframe_deletion)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(Y128F)
Single nucleotide variant
(missense variant +1 more)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(C235R +1 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(R199S +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
LOC129929541, SDHB
Single nucleotide variant
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
(P49S)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
Single nucleotide variant
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
(M71T)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(T232R +1 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(A29S)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
Duplication
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
Deletion
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
LOC129929542, SDHB
Single nucleotide variant
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
(A112V)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
Single nucleotide variant
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
Single nucleotide variant
(synonymous variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
Single nucleotide variant
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
(N145S +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
SDHB
Single nucleotide variant
(synonymous variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
Single nucleotide variant
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
LOC129929542, SDHB
Single nucleotide variant
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
Single nucleotide variant
(synonymous variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
Single nucleotide variant
(synonymous variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
Single nucleotide variant
(synonymous variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
Single nucleotide variant
(synonymous variant +1 more)
Pheochromocytoma
+2 more
GLikely benign
SDHB
Single nucleotide variant
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
(R115L)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(Q30H)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
LOC129929541, SDHB
Single nucleotide variant
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
LOC129929542, SDHB
Single nucleotide variant
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
(D124N +1 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(P241L +1 more)
Single nucleotide variant
(missense variant)
Hereditary pheochromocytoma-paraganglioma
+3 more
GUncertain significance
SDHB
(K78N)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
Single nucleotide variant
(synonymous variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
(G203* +1 more)
Single nucleotide variant
(nonsense)
Pheochromocytoma
+2 more
GPathogenic
SDHB
(D206H +1 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+2 more
GUncertain significance
SDHB
(Q235* +1 more)
Single nucleotide variant
(nonsense)
Pheochromocytoma
+2 more
GPathogenic
SDHB
Single nucleotide variant
(intron variant)
Pheochromocytoma
+2 more
GLikely benign
SDHB
Single nucleotide variant
(synonymous variant +1 more)
Pheochromocytoma
+2 more
GLikely benign
SDHB
Single nucleotide variant
(synonymous variant)
Pheochromocytoma
+2 more
GLikely benign
Format
Items per page
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