Have questions? Visit https://www.reddit.com/r/SNPedia

rs6457477

From SNPedia

Orientationplus
Stabilizedplus
Make rs6457477(C;C)
Make rs6457477(C;T)
Make rs6457477(T;T)
ReferenceGRCh37 37.1/131
Chromosome6
Position31977391
GeneTNXA
is asnp
is mentioned by
dbSNPrs6457477
ebirs6457477
HLIrs6457477
Exacrs6457477
Varsomers6457477
Maprs6457477
PheGenIrs6457477
hapmaprs6457477
1000 genomesrs6457477
hgdprs6457477
ensemblrs6457477
gopubmedrs6457477
geneviewrs6457477
scholarrs6457477
googlers6457477
pharmgkbrs6457477
gwascentralrs6457477
openSNPrs6457477
23andMers6457477
23andMe allrs6457477
SNP Nexus

SNPshotrs6457477
SNPdbers6457477
MSV3drs6457477
GWAS Ctlgrs6457477
Max Magnitude
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