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rs137852901

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852901(A;G)
Make rs137852901(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position79983915
GeneANTXR2
is asnp
is mentioned by
dbSNPrs137852901
ebirs137852901
HLIrs137852901
Exacrs137852901
Varsomers137852901
Maprs137852901
PheGenIrs137852901
hapmaprs137852901
1000 genomesrs137852901
hgdprs137852901
ensemblrs137852901
gopubmedrs137852901
geneviewrs137852901
scholarrs137852901
googlers137852901
pharmgkbrs137852901
gwascentralrs137852901
openSNPrs137852901
23andMers137852901
23andMe allrs137852901
SNP Nexus

SNPshotrs137852901
SNPdbers137852901
MSV3drs137852901
GWAS Ctlgrs137852901
Max Magnitude0
OMIM608041
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137852901(G,T;G,T)
Alt rs137852901(G,T;G,T)
Reference rs137852901(A;A)
Significance Pathogenic
Disease Hyaline fibromatosis syndrome
Variation info
Gene ANTXR2
CLNDBN Hyaline fibromatosis syndrome
Reversed 1
HGVS NC_000004.11:g.80905069T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000002717.2,