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rs35445429

From SNPedia

Merged intors4959083
Orientationplus
Stabilizedplus
Make rs35445429(C;C)
Make rs35445429(C;T)
Make rs35445429(T;T)
ReferenceGRCh37 37.1/131
Chromosome6
Position31976916
GeneTNXA
is asnp
is mentioned by
dbSNPrs35445429
ebirs35445429
HLIrs35445429
Exacrs35445429
Varsomers35445429
Maprs35445429
PheGenIrs35445429
hapmaprs35445429
1000 genomesrs35445429
hgdprs35445429
ensemblrs35445429
gopubmedrs35445429
geneviewrs35445429
scholarrs35445429
googlers35445429
pharmgkbrs35445429
gwascentralrs35445429
openSNPrs35445429
23andMers35445429
23andMe allrs35445429
SNP Nexus

SNPshotrs35445429
SNPdbers35445429
MSV3drs35445429
GWAS Ctlgrs35445429
StatusMerged into rs4959083
Max Magnitude
Venter snp
Source plos
Gene TNXB
allele T
frequency
sift TOLERATED
HuRef 1103652827630
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.


Neighborrs36007903
Distance10