Rs6457477

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is asnp
is mentioned by
dbSNPrs6457477
hapmaprs6457477
hgdprs6457477
ensemblrs6457477
gopubmedrs6457477
scholarrs6457477
googlers6457477
pharmgkbrs6457477
hgvbaseg2prs6457477
medrefsnprs6457477
23andMers6457477
SNP Nexus

GeneTNXB
Chromosome6
Orientationplus
Position32085368
GenotypeEffect
rs6457477(C;C)*?
rs6457477(C;T)*?
rs6457477(T;T)*?



Venter snp
Source plos
Gene TNXB
allele T
frequency
sift AFFECT FUNCTION
HuRef 1103652827635
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.


Neighborrs6941704
Distance224
Neighborrs10456399
Distance398