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rs387906853

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906853(A;A)
Make rs387906853(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position67181297
GeneSMAD3
is asnp
is mentioned by
dbSNPrs387906853
ebirs387906853
HLIrs387906853
Exacrs387906853
Varsomers387906853
Maprs387906853
PheGenIrs387906853
hapmaprs387906853
1000 genomesrs387906853
hgdprs387906853
ensemblrs387906853
gopubmedrs387906853
geneviewrs387906853
scholarrs387906853
googlers387906853
pharmgkbrs387906853
gwascentralrs387906853
openSNPrs387906853
23andMers387906853
23andMe allrs387906853
SNP Nexus

SNPshotrs387906853
SNPdbers387906853
MSV3drs387906853
GWAS Ctlgrs387906853
Max Magnitude0
ClinVar
Risk rs387906853(A;A)
Alt rs387906853(A;A)
Reference rs387906853(G;G)
Significance Pathogenic
Disease Loeys-Dietz syndrome 3 not specified
Variation info
Gene SMAD3
CLNDBN Loeys-Dietz syndrome 3 not specified
Reversed 0
HGVS NC_000015.9:g.67473635G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023246.3, RCV000200841.2,