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rs863223750

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223750(G;T)
Make rs863223750(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position67066236
GeneSMAD3
is asnp
is mentioned by
dbSNPrs863223750
ebirs863223750
HLIrs863223750
Exacrs863223750
Varsomers863223750
Maprs863223750
PheGenIrs863223750
hapmaprs863223750
1000 genomesrs863223750
hgdprs863223750
ensemblrs863223750
gopubmedrs863223750
geneviewrs863223750
scholarrs863223750
googlers863223750
pharmgkbrs863223750
gwascentralrs863223750
openSNPrs863223750
23andMers863223750
23andMe allrs863223750
SNP Nexus

SNPshotrs863223750
SNPdbers863223750
MSV3drs863223750
GWAS Ctlgrs863223750
Max Magnitude0
ClinVar
Risk rs863223750(T;T)
Alt rs863223750(T;T)
Reference rs863223750(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SMAD3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.67358574G>T
CLNSRC
CLNACC RCV000198731.1,