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rs797045029

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797045029(C;C)
Make rs797045029(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position80069491
GeneANTXR2
is asnp
is mentioned by
dbSNPrs797045029
ebirs797045029
HLIrs797045029
Exacrs797045029
Varsomers797045029
Maprs797045029
PheGenIrs797045029
hapmaprs797045029
1000 genomesrs797045029
hgdprs797045029
ensemblrs797045029
gopubmedrs797045029
geneviewrs797045029
scholarrs797045029
googlers797045029
pharmgkbrs797045029
gwascentralrs797045029
openSNPrs797045029
23andMers797045029
23andMe allrs797045029
SNP Nexus

SNPshotrs797045029
SNPdbers797045029
MSV3drs797045029
GWAS Ctlgrs797045029
Max Magnitude0
ClinVar
Risk rs797045029(C;C)
Alt rs797045029(C;C)
Reference rs797045029(T;T)
Significance Probable-Pathogenic
Disease Hyaline fibromatosis syndrome
Variation info
Gene ANTXR2
CLNDBN Hyaline fibromatosis syndrome
Reversed 1
HGVS NC_000004.11:g.80990645A>G
CLNSRC Baylor College of Medicine
CLNACC RCV000191062.1,