SHH, sonic hedgehog signaling molecule, 6469

N. diseases: 303; N. variants: 44
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894049
rs104894049
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C1840235
Disease:
SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR
A 0.810 CausalMutation CLINVAR
dbSNP: rs104894040
rs104894040
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C1840529
Disease:
HOLOPROSENCEPHALY 3
G 0.800 CausalMutation CLINVAR
dbSNP: rs104894040
rs104894040
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C1840529
Disease:
HOLOPROSENCEPHALY 3
C 0.800 CausalMutation CLINVAR
dbSNP: rs104894042
rs104894042
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C1840529
Disease:
HOLOPROSENCEPHALY 3
T 0.800 CausalMutation CLINVAR
dbSNP: rs104894043
rs104894043
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C1840529
Disease:
HOLOPROSENCEPHALY 3
T 0.800 CausalMutation CLINVAR
dbSNP: rs104894048
rs104894048
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C1840529
Disease:
HOLOPROSENCEPHALY 3
C 0.800 CausalMutation CLINVAR
dbSNP: rs104894050
rs104894050
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C1840529
Disease:
HOLOPROSENCEPHALY 3
A 0.800 CausalMutation CLINVAR
dbSNP: rs104894052
rs104894052
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C1840235
Disease:
SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR
G 0.800 CausalMutation CLINVAR
dbSNP: rs267607047
rs267607047
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C1840529
Disease:
HOLOPROSENCEPHALY 3
T 0.800 CausalMutation CLINVAR
dbSNP: rs587778792
rs587778792
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C0079541
Disease:
Holoprosencephaly
G 0.710 CausalMutation CLINVAR
dbSNP: rs587778799
rs587778799
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C0079541
Disease:
Holoprosencephaly
G 0.710 CausalMutation CLINVAR
dbSNP: rs104894040
rs104894040
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C0079541
Disease:
Holoprosencephaly
G 0.700 CausalMutation CLINVAR
dbSNP: rs104894040
rs104894040
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C0079541
Disease:
Holoprosencephaly
C 0.700 CausalMutation CLINVAR
dbSNP: rs104894042
rs104894042
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C0079541
Disease:
Holoprosencephaly
T 0.700 CausalMutation CLINVAR
dbSNP: rs104894043
rs104894043
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C0079541
Disease:
Holoprosencephaly
T 0.700 CausalMutation CLINVAR
dbSNP: rs104894044
rs104894044
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C1840529
Disease:
HOLOPROSENCEPHALY 3
A 0.700 CausalMutation CLINVAR
dbSNP: rs104894044
rs104894044
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C0079541
Disease:
Holoprosencephaly
A 0.700 CausalMutation CLINVAR
dbSNP: rs104894045
rs104894045
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C1840529
Disease:
HOLOPROSENCEPHALY 3
A 0.700 CausalMutation CLINVAR
dbSNP: rs104894045
rs104894045
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C0079541
Disease:
Holoprosencephaly
A 0.700 CausalMutation CLINVAR
dbSNP: rs104894046
rs104894046
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C1840529
Disease:
HOLOPROSENCEPHALY 3
A 0.700 CausalMutation CLINVAR
dbSNP: rs104894046
rs104894046
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C0079541
Disease:
Holoprosencephaly
A 0.700 CausalMutation CLINVAR
dbSNP: rs104894048
rs104894048
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C0079541
Disease:
Holoprosencephaly
C 0.700 CausalMutation CLINVAR
dbSNP: rs104894050
rs104894050
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C0079541
Disease:
Holoprosencephaly
A 0.700 CausalMutation CLINVAR
dbSNP: rs104894051
rs104894051
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C1840529
Disease:
HOLOPROSENCEPHALY 3
A 0.700 CausalMutation CLINVAR
dbSNP: rs104894051
rs104894051
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C0079541
Disease:
Holoprosencephaly
A 0.700 CausalMutation CLINVAR