Rs10456399

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is asnp
is mentioned by
dbSNPrs10456399
hapmaprs10456399
hgdprs10456399
ensemblrs10456399
gopubmedrs10456399
scholarrs10456399
googlers10456399
pharmgkbrs10456399
hgvbaseg2prs10456399
medrefsnprs10456399
23andMers10456399
SNP Nexus

GeneTNXB
Chromosome6
Orientationplus
Position32085766
GenotypeEffect
rs10456399(A;A)*?
rs10456399(A;G)*?
rs10456399(G;G)*?



Venter snp
Source plos
Gene TNXB
allele G
frequency
sift AFFECT FUNCTION
HuRef 1103652827645
Disease Association Defects in TNXB are the cause of Ehlers-Danlos-like syndrome (MIM:606408). This clinically distinct form of Ehlers- Danlos syndrome is characterized by hyperextensible skin, hypermobile joints, and tissue fragility, but it lacks atrophic scars and delayed wound healing. Inheritance is autosomal recessive.


Neighborrs6457477
Distance398
Neighborrs1135809
Distance209