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rs766024374

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs766024374(A;A)
Make rs766024374(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position218346914
GeneTGFB2, TGFB2-AS1
is asnp
is mentioned by
dbSNPrs766024374
dbSNP (classic)rs766024374
ClinGenrs766024374
ebirs766024374
HLIrs766024374
Exacrs766024374
Gnomadrs766024374
Varsomers766024374
LitVarrs766024374
Maprs766024374
PheGenIrs766024374
Biobankrs766024374
1000 genomesrs766024374
hgdprs766024374
ensemblrs766024374
geneviewrs766024374
scholarrs766024374
googlers766024374
pharmgkbrs766024374
gwascentralrs766024374
openSNPrs766024374
23andMers766024374
23andMe allrs766024374
SNPshotrs766024374
SNPdbers766024374
MSV3drs766024374
GWAS Ctlgrs766024374
Max Magnitude0
ClinVar
Risk rs766024374(A;A) rs766024374(T;T)
Alt rs766024374(A;A) rs766024374(T;T)
Reference Rs766024374(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TGFB2 TGFB2-AS1
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.218520256C>A
CLNSRC
CLNACC RCV000428017.1,