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rs772339721

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs772339721(A;T)
Make rs772339721(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position99137964
GeneTGFBR1
is asnp
is mentioned by
dbSNPrs772339721
dbSNP (classic)rs772339721
ClinGenrs772339721
ebirs772339721
HLIrs772339721
Exacrs772339721
Gnomadrs772339721
Varsomers772339721
LitVarrs772339721
Maprs772339721
PheGenIrs772339721
Biobankrs772339721
1000 genomesrs772339721
hgdprs772339721
ensemblrs772339721
geneviewrs772339721
scholarrs772339721
googlers772339721
pharmgkbrs772339721
gwascentralrs772339721
openSNPrs772339721
23andMers772339721
SNPshotrs772339721
SNPdbers772339721
MSV3drs772339721
GWAS Ctlgrs772339721
Max Magnitude0
ClinVar
Risk rs772339721(G;G) rs772339721(T;T)
Alt rs772339721(G;G) rs772339721(T;T)
Reference Rs772339721(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFBR1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.101900246A>T
CLNSRC
CLNACC RCV000483348.1,