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rs10456399

From SNPedia

Orientationplus
Stabilizedplus
Make rs10456399(A;A)
Make rs10456399(A;G)
Make rs10456399(G;G)
ReferenceGRCh37.p5 37.3/135
Chromosome6
Position31977789
GeneTNXB
is asnp
is mentioned by
dbSNPrs10456399
ebirs10456399
HLIrs10456399
Exacrs10456399
Varsomers10456399
Maprs10456399
PheGenIrs10456399
hapmaprs10456399
1000 genomesrs10456399
hgdprs10456399
ensemblrs10456399
gopubmedrs10456399
geneviewrs10456399
scholarrs10456399
googlers10456399
pharmgkbrs10456399
gwascentralrs10456399
openSNPrs10456399
23andMers10456399
23andMe allrs10456399
SNP Nexus

SNPshotrs10456399
SNPdbers10456399
MSV3drs10456399
GWAS Ctlgrs10456399
Max Magnitude
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