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

rs137852903

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852903(G;G)
Make rs137852903(G;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position80008576
GeneANTXR2
is asnp
is mentioned by
dbSNPrs137852903
ebirs137852903
HLIrs137852903
Exacrs137852903
Varsomers137852903
Maprs137852903
PheGenIrs137852903
hapmaprs137852903
1000 genomesrs137852903
hgdprs137852903
ensemblrs137852903
gopubmedrs137852903
geneviewrs137852903
scholarrs137852903
googlers137852903
pharmgkbrs137852903
gwascentralrs137852903
openSNPrs137852903
23andMers137852903
23andMe allrs137852903
SNP Nexus

SNPshotrs137852903
SNPdbers137852903
MSV3drs137852903
GWAS Ctlgrs137852903
Max Magnitude0
OMIM608041
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137852903(G;G)
Alt rs137852903(G;G)
Reference rs137852903(T;T)
Significance Pathogenic
Disease Hyaline fibromatosis syndrome
Variation info
Gene ANTXR2
CLNDBN Hyaline fibromatosis syndrome
Reversed 1
HGVS NC_000004.11:g.80929730A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000002719.2,