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rs281865484

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281865484(A;A)
Make rs281865484(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position41348306
GeneTGFB1
is asnp
is mentioned by
dbSNPrs281865484
ebirs281865484
HLIrs281865484
Exacrs281865484
Varsomers281865484
Maprs281865484
PheGenIrs281865484
hapmaprs281865484
1000 genomesrs281865484
hgdprs281865484
ensemblrs281865484
gopubmedrs281865484
geneviewrs281865484
scholarrs281865484
googlers281865484
pharmgkbrs281865484
gwascentralrs281865484
openSNPrs281865484
23andMers281865484
23andMe allrs281865484
SNP Nexus

SNPshotrs281865484
SNPdbers281865484
MSV3drs281865484
GWAS Ctlgrs281865484
Max Magnitude0
ClinVar
Risk rs281865484(A;A)
Alt rs281865484(A;A)
Reference rs281865484(G;G)
Significance Pathogenic
Disease Diaphyseal dysplasia
Variation info
Gene TGFB1
CLNDBN Diaphyseal dysplasia
Reversed 1
HGVS NC_000019.10:g.41348306C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000032148.1,