Gene: SDHD ×
Source: CURATED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060503770
rs1060503770
SDHD
T 0.710 CausalMutation CLINVAR

dbSNP: rs104894310
rs104894310
SDHD ; TIMM8B
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060503769
rs1060503769
SDHD
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060503773
rs1060503773
SDHD
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1566690018
rs1566690018
SDHD ; TIMM8B
C 0.700 CausalMutation CLINVAR

dbSNP: rs587776648
rs587776648
SDHD
T 0.700 CausalMutation CLINVAR

dbSNP: rs587782210
rs587782210
SDHD ; TIMM8B
A 0.700 CausalMutation CLINVAR

dbSNP: rs864321644
rs864321644
SDHD
C 0.700 GeneticVariation CLINVAR

dbSNP: rs876658477
rs876658477
SDHD
G 0.700 GeneticVariation CLINVAR

dbSNP: rs878854589
rs878854589
SDHD ; TIMM8B
TC 0.700 CausalMutation CLINVAR

dbSNP: rs878854590
rs878854590
SDHD
T 0.700 CausalMutation CLINVAR

dbSNP: rs878854591
rs878854591
SDHD
T 0.700 CausalMutation CLINVAR

dbSNP: rs80338844
rs80338844
SDHD
T 0.800 CausalMutation CLINVAR Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. 10657297

2000
dbSNP: rs104894302
rs104894302
SDHD
T 0.700 GeneticVariation CLINVAR Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. 10657297

2000
dbSNP: rs80338843
rs80338843
SDHD ; TIMM8B
T 0.700 CausalMutation CLINVAR Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. 10657297

2000
dbSNP: rs80338843
rs80338843
SDHD ; TIMM8B
T 0.700 CausalMutation CLINVAR Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma. 11156372

2000
dbSNP: rs397514034
rs397514034
SDHD ; TIMM8B
A 0.700 CausalMutation CLINVAR Germline SDHD mutation in familial phaeochromocytoma. 11323050

2001
dbSNP: rs104894304
rs104894304
SDHD
G 0.700 CausalMutation CLINVAR Novel mutations and the emergence of a common mutation in the SDHD gene causing familial paraganglioma. 11343322

2001
dbSNP: rs80338844
rs80338844
SDHD
T 0.800 CausalMutation CLINVAR Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss. 11391796

2001
dbSNP: rs104894307
rs104894307
SDHD ; TIMM8B
T 0.700 CausalMutation CLINVAR Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss. 11391796

2001
dbSNP: rs387906358
rs387906358
SDHD
A 0.700 CausalMutation CLINVAR Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss. 11391796

2001
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
A 0.700 CausalMutation CLINVAR Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss. 11391796

2001
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
C 0.700 CausalMutation CLINVAR Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss. 11391796

2001
dbSNP: rs104894306
rs104894306
SDHD ; TIMM8B
T 0.700 CausalMutation CLINVAR Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene. 11391798

2001
dbSNP: rs1050032491
rs1050032491
SDHD
A 0.700 CausalMutation CLINVAR Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene. 11391798

2001