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rs36007903

From SNPedia

Merged intors4959084
Orientationplus
Stabilizedplus
Make rs36007903(C;C)
Make rs36007903(C;T)
Make rs36007903(T;T)
ReferenceGRCh37 37.1/131
Chromosome6
Position31976926
GeneTNXA
is asnp
is mentioned by
dbSNPrs36007903
ebirs36007903
HLIrs36007903
Exacrs36007903
Varsomers36007903
Maprs36007903
PheGenIrs36007903
hapmaprs36007903
1000 genomesrs36007903
hgdprs36007903
ensemblrs36007903
gopubmedrs36007903
geneviewrs36007903
scholarrs36007903
googlers36007903
pharmgkbrs36007903
gwascentralrs36007903
openSNPrs36007903
23andMers36007903
23andMe allrs36007903
SNP Nexus

SNPshotrs36007903
SNPdbers36007903
MSV3drs36007903
GWAS Ctlgrs36007903
StatusMerged into rs4959084
Max Magnitude
Venter snp
Source plos
Gene TNXB
allele T
frequency
sift AFFECT FUNCTION
HuRef 1103652827631
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.


Neighborrs35445429
Distance10
Neighborrs6941704
Distance241