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rs137852902

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852902(A;A)
Make rs137852902(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position80055996
GeneANTXR2
is asnp
is mentioned by
dbSNPrs137852902
ebirs137852902
HLIrs137852902
Exacrs137852902
Varsomers137852902
Maprs137852902
PheGenIrs137852902
hapmaprs137852902
1000 genomesrs137852902
hgdprs137852902
ensemblrs137852902
gopubmedrs137852902
geneviewrs137852902
scholarrs137852902
googlers137852902
pharmgkbrs137852902
gwascentralrs137852902
openSNPrs137852902
23andMers137852902
23andMe allrs137852902
SNP Nexus

SNPshotrs137852902
SNPdbers137852902
MSV3drs137852902
GWAS Ctlgrs137852902
Max Magnitude0
OMIM608041
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137852902(A;A)
Alt rs137852902(A;A)
Reference rs137852902(G;G)
Significance Pathogenic
Disease Hyaline fibromatosis syndrome
Variation info
Gene ANTXR2
CLNDBN Hyaline fibromatosis syndrome
Reversed 1
HGVS NC_000004.11:g.80977150C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002718.2,